128027983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28397178-T-C

128027996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28397165-C-T

http://identifiers.org/hco/6/GRCh38#128027997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28397164-A-C

128028107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28397072-G-A

http://identifiers.org/hco/6/GRCh38#128028124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28397055-C-A

128029867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28396847-G-A

128029939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28396772-G-A

128030300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28396473-A-G

128030809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28395922-T-C

128030911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28395836-G-A

128031326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28395361-T-C

128031370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28395238-C-T

128031571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28395091-T-C

128031691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28394982-G-C

128031888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28394826-A-G

128032536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28394299-T-C

128032560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28394274-T-C

128032855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28393640-C-T

http://identifiers.org/hco/6/GRCh38#128032881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28393616-C-A

128033157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28393394-G-A

128033209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28393343-T-C

128033209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28393343-T-G

128033301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28393269-T-A

128034118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28393049-C-T

128034196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28392981-T-C

128034259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28392917-G-A

128034265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28392909-T-C

128034366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28392827-A-G

128034480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28392714-T-A

128035043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28392227-A-G

128036352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28391756-A-T

128036506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28391612-C-T

128037172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28391228-T-C

128037172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28391228-T-G

128037263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28391135-A-G

128039599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28390432-G-C

128040276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28389876-A-G

128040600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28389628-A-G

128040701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28389538-A-T

128040987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28389297-T-C

128041141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28389149-T-A

128041186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28389098-C-T

128041555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28388727-T-C

128041866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28387948-C-T

128041970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28387851-T-A

128042134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28387687-T-C

128042153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28387667-C-T

128042363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28387292-C-T

128042538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28387118-A-G

128042706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28386985-T-C

128043033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28386759-A-G

128043142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28386669-C-T

128043182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28386626-A-G

128043183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28386625-T-C

128043188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28386620-C-G

128043347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28386480-G-C

128043540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28386285-T-A

128043540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28386285-T-C

128043569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28386251-C-G

128044001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28385623-G-A

http://identifiers.org/hco/6/GRCh38#128044167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28385115-C-A

128044215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28385067-C-T

128044389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28384890-A-G

128045466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28384094-C-T

128045781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28383745-T-C

128045937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28383612-G-A

http://identifiers.org/hco/6/GRCh38#128045942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28383607-A-C

http://identifiers.org/hco/6/GRCh38#128046079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28383471-A-C

128046199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28383353-T-C

128046233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28383305-A-T

128046399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28383130-T-C

http://identifiers.org/hco/6/GRCh38#128046466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28383064-C-A

128046466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28383064-C-T

128046905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28382672-T-G

128046960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28382616-T-C

128047034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28382543-G-A

128047039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28382538-T-C

128047039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28382538-T-G

128049452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28382068-T-A

128049532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28381998-T-C

128049554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28381977-T-G

128053049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -T-A

128053049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -T-C

http://identifiers.org/hco/6/GRCh38#128055168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28380644-A-C

128055207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28380605-T-C

128055249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28380560-C-G

128056216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28379862-T-C

128056224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28379852-G-A

128056927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28379456-A-G

128057012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28379370-C-G

128059894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28377452-T-C

128060019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28377339-T-C

128060467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28376986-T-C

128060513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28376938-C-G

128060513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28376938-C-T

128060762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28376723-T-C

128061439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28376303-A-G

128061616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28376145-A-G

http://identifiers.org/hco/6/GRCh38#128061814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28375976-A-C

128061915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28375876-G-A

128061938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28375848-T-C

http://identifiers.org/hco/6/GRCh38#128062068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28375719-C-A

128062117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28375671-G-T

128062636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28375133-T-C

128062737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28375053-G-T

http://identifiers.org/hco/6/GRCh38#128062755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28375035-C-A

128062755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28375035-C-T

128063037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28374822-T-G

128063255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28374626-T-C

128063273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28374607-T-C

128063378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28374499-G-T

128063389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28374487-G-A

128063457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28374406-G-T

128063484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28374379-G-T

128063487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28374376-A-G

128063539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28374323-G-C

128063745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28374105-A-T

128063963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28373901-C-T

128063998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28373866-G-A

128064145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28373732-C-T

128064314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28373500-C-T

128064464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28373343-C-T

128064491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28373320-C-T

http://identifiers.org/hco/6/GRCh38#128064549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28373264-A-C

128064549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28373264-A-T

http://identifiers.org/hco/6/GRCh38#128064612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28373204-C-A

128064612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28373204-C-T

http://identifiers.org/hco/6/GRCh38#128064698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28373084-C-A

128064698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28373084-C-T

128064712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28373070-A-G

128064842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28372857-T-C

128064842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28372857-T-G

128065066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28372650-T-C

128065614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28371546-T-A

128065614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28371546-T-C

128065709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28371454-G-A

128065950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28371187-G-A

128066320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28370336-C-T

128066340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28370316-T-G

http://identifiers.org/hco/6/GRCh38#128066367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28370289-C-A

128066452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28370210-G-T

128066835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28369868-T-C

128067288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28369417-G-C

128067289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28369416-C-T

128067295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28369410-T-C

128067493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28369211-A-G

128067661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28369039-G-A

128067676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28369024-G-A

http://identifiers.org/hco/6/GRCh38#128067688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28369012-C-A

128067688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28369012-C-G

128067688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28369012-C-T

128067691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28369009-A-G

128067691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28369009-A-T

128067851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368867-G-A

128067851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368867-G-C

128067851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368867-G-T

128067856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368862-T-A

128067856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368862-T-C

128067856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368862-T-G

http://identifiers.org/hco/6/GRCh38#128067860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28368858-A-C

128067870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368839-A-G

128067870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368839-A-T

128067871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368838-G-T

128067880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368829-T-A

128067880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368829-T-C

128067880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368829-T-G

http://identifiers.org/hco/6/GRCh38#128067904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28368805-A-C

128067904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368805-A-T

128067944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368785-T-A

128067944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368785-T-C

128067944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368785-T-G

128068215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368506-G-A

128068236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368485-C-T

128068531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368188-A-G

128068531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368188-A-T

128068608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368133-A-G

128068654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28368087-A-G

http://identifiers.org/hco/6/GRCh38#128069320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28367233-C-A

128069401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28367163-T-C

128069547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28366990-T-C

128069563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28366974-G-A

128069606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28366934-C-T

http://identifiers.org/hco/6/GRCh38#128069719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28366818-C-A

128069719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28366818-C-T

128069761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28366785-A-G

128069835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28366688-T-C

128069835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28366688-T-G

128070131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28366457-A-G

128070143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28366445-T-C

128070154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28366434-T-C

http://identifiers.org/hco/6/GRCh38#128070650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28366006-C-A

128070650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28366006-C-T

128070793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28365873-T-G

128071144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28365558-G-T

128071185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28365516-T-C

128071587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28365052-C-T

128071773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28364874-T-C

128075702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28362457-A-T

http://identifiers.org/hco/6/GRCh38#128075786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28362360-C-A

128075802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28362344-T-A

128075817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28362333-A-G

128075845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28362306-A-G

128075845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28362306-A-T

128075866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28362285-T-C

128075879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28362272-A-T

128075898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28362253-G-A

128076369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28361829-G-C

128076501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28361611-A-G

128076582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28361300-T-C

128076704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28361159-T-C

128076704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28361159-T-G

128076737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28361107-A-G

128076993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360808-G-A

128076995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360806-G-A

128077024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360783-T-C

128077043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360764-A-G

http://identifiers.org/hco/6/GRCh38#128077111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28360456-A-C

128077145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360423-T-G

128077164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360405-A-T

http://identifiers.org/hco/6/GRCh38#128077166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28360403-A-C

http://identifiers.org/hco/6/GRCh38#128077210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28360359-A-C

128077213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360356-T-C

128077250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360310-C-G

128077473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360097-T-C

128077488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360083-A-G

128077522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360053-T-G

128077555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360042-G-A

http://identifiers.org/hco/6/GRCh38#128077590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28360007-C-A

128077595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360003-G-T

128077596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28360002-T-C

128077720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28359878-T-G

http://identifiers.org/hco/6/GRCh38#128077730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28359868-A-C

128077958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28359643-A-G

http://identifiers.org/hco/6/GRCh38#128078932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28359168-A-C

128078938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28359162-A-G

128078938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28359162-A-T

128079616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28358527-G-A

128079655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28358452-T-C

128079799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28358315-A-G

128081403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28352171-A-T

http://identifiers.org/hco/6/GRCh38#128081412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28352162-A-C

128081697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28351969-A-G

128082298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28351414-T-G

128082375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28351342-G-T

128082410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28351307-C-T

128082597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28351120-T-C

http://identifiers.org/hco/6/GRCh38#128082625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28351092-C-A

128082625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28351092-C-T

128082713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28351013-G-A

128082713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28351013-G-C

128082713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28351013-G-T

128082828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28350892-A-T

128083083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28350386-T-C

128083236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28350172-G-C

128083333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28350076-T-G

128083526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28349887-G-A

128083526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28349887-G-T

http://identifiers.org/hco/6/GRCh38#128083611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28349147-A-C

128083611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28349147-A-G

128083613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28349145-T-A

128083613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28349145-T-G

128083737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 28349029-T-C

128083831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 28348936-A-G

128083854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28348916-A-G

128083993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28347153-G-A

128083995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28347151-T-A

128084126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28347017-T-C

128084126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28347017-T-G

128084142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28347001-C-T

128084313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28346833-T-G

128084314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28346832-G-A

128084434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28346713-G-A

128084651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28346216-G-A

128084780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28346105-A-T

128084786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28346099-T-A

128084934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28345957-G-A

128084934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28345957-G-T

128085044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28345847-T-C

http://identifiers.org/hco/6/GRCh38#128085111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28345780-C-A

128085167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28345724-C-G

128085167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28345724-C-T

128085237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28345687-G-A

128085260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28345667-C-T

128085281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28345645-G-T