69984249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144293727-C-G

69984401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144293622-T-A

69984401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144293622-T-G

69984711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144293381-C-G

69984711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144293381-C-T

http://identifiers.org/hco/11/GRCh38#69984984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144293168-A-C

69985419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144292768-T-C

69985458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144292727-C-T

69985502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144292676-C-T

69985565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144292583-T-C

69985882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144292330-G-T

69986206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144292159-G-A

69986206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144292159-G-T

http://identifiers.org/hco/11/GRCh38#69986447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144291950-C-A

69986447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144291950-C-T

69986478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144291898-G-A

69986511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144291826-T-A

69986626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144291692-A-G

http://identifiers.org/hco/11/GRCh38#69986885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144291475-A-C

69987238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144291250-C-G

69987693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144290987-C-T

69987798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144290882-G-A

69987929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144290759-C-T

69987958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144290730-T-C

69988032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144290640-G-A

69988316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144290367-G-C

http://identifiers.org/hco/11/GRCh38#69988434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144290282-C-A

69988434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144290282-C-T

69990781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144288082-A-G

69990794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144288069-G-T

69990911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144287974-G-T

69990986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144287835-C-T

69991020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144287801-C-T

69991154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144287674-G-A

69991154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144287674-G-C

69992274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144286419-T-A

69992281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144286412-C-G

69992553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144285999-C-T

69993085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144285508-A-G

69993209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144285398-C-T

69993226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144285382-A-G

69993259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144285352-G-C

69993282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144285329-C-T

69993307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144285304-T-C

69993308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144285303-G-A

69993391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144285226-T-A

69993636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144284872-G-C

69993679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144284842-A-G

http://identifiers.org/hco/11/GRCh38#69994091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144284338-A-C

69994091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144284338-A-G

69994226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144284247-A-G

69994411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144284068-G-A

69994532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144283666-T-C

69999816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144277040-T-G

70005433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144274069-G-A

70005501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144274001-C-T

70010616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144270451-G-A

70011308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144269799-G-T

70011705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144269455-G-A

70012167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144269047-C-T

70012320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144268887-A-G

70020482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144266974-C-T

70020632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144266842-G-A

70020632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144266842-G-C

70020738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144266741-G-A

70020738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144266741-G-T

http://identifiers.org/hco/11/GRCh38#70020816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144266673-C-A

70020816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144266673-C-T

70020849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144266635-A-G

70021043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144266476-A-G

70021797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144265783-C-T

70021854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144265728-G-A

70022705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144265284-G-A

70022939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144265084-G-C

http://identifiers.org/hco/11/GRCh38#70022974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144265055-C-A

70022974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144265055-C-G

70023246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144264836-T-G

70023263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144264823-G-A

70023290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144264794-G-A

70023290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144264794-G-T

70023292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144264792-A-G

70023326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144264759-A-T

70023605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144264537-T-A

70024141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144263922-C-T

70024294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144263769-A-T

http://identifiers.org/hco/11/GRCh38#70047779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144251983-C-A

70047779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144251983-C-T

70047963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144251793-C-T

70048472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144251294-G-A

70048472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144251294-G-T

70048929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, undefined
orthologous variants: 144250566-G-A

70049191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144250332-G-A

70049224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144250305-T-C

70049286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144250245-G-A

70049301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144250230-G-A

70049369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144250162-T-G

70053743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144249387-T-G

70053874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144249233-T-C

70054042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144249138-T-C

http://identifiers.org/hco/11/GRCh38#70054070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144249114-A-C

70054459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144248639-T-A

70063607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144244350-A-G

70063645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144244312-A-G

70063708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144244235-A-G

http://identifiers.org/hco/11/GRCh38#70063819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144244127-C-A

70064061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243947-G-A

70064061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243947-G-T

70064130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243876-A-G

http://identifiers.org/hco/11/GRCh38#70064161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144243828-C-A

70064161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243828-C-T

70064408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243648-T-A

70064408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243648-T-C

70064408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243648-T-G

http://identifiers.org/hco/11/GRCh38#70064446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144243605-C-A

70064522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243531-T-C

70064616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243463-T-C

http://identifiers.org/hco/11/GRCh38#70064628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144243452-C-A

70064705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243366-G-A

70064705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243366-G-T

http://identifiers.org/hco/11/GRCh38#70064715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144243356-C-A

70064715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243356-C-T

70064793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243298-T-C

70064793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243298-T-G

70064866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243225-C-T

70064874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243217-T-C

70065001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144243104-G-A

70067802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144241354-T-C

70067823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144241333-G-C

70067878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144241287-T-G

70068211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144240981-G-T

70073550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144238899-T-C

70073563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144238885-C-G

70073931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144238459-G-A

70074188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144238291-T-A

70075058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144235933-G-T

70075091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144235900-G-A

70075102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144235889-T-C

70075145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144235850-T-G

http://identifiers.org/hco/11/GRCh38#70075190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144235809-C-A

70075190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144235809-C-G

http://identifiers.org/hco/11/GRCh38#70075202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144235797-C-A

70076025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144234868-T-C

http://identifiers.org/hco/11/GRCh38#70076756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144233943-C-A

70076757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144233942-C-T

70076927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144233795-C-T

70077210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144233551-T-C

70077461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144233373-A-G

70078646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense variant
orthologous variants: 144232437-G-A

70078646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense variant
orthologous variants: 144232437-G-C

70078646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense variant
orthologous variants: 144232437-G-T

70078662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense variant
orthologous variants: 144232421-T-A

70078662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense variant
orthologous variants: 144232421-T-C

70078662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense variant
orthologous variants: 144232421-T-G

http://identifiers.org/hco/11/GRCh38#70078737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144232333-C-A

70078737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144232333-C-G

70078737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144232333-C-T

70078751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, undefined
orthologous variants: 144232304-G-A

70078751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, undefined
orthologous variants: 144232304-G-C

70078751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, undefined
orthologous variants: 144232304-G-T

70078770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144232286-A-G

http://identifiers.org/hco/11/GRCh38#70078797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144232237-C-A

70078797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144232237-C-T

http://identifiers.org/hco/11/GRCh38#70078805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144232205-A-C

http://identifiers.org/hco/11/GRCh38#70078826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144232184-C-A

70078826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144232184-C-T

70079497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144231350-T-G

70079505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144231342-G-A

70079662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144231219-C-T

70079686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144231165-C-T

70080216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, undefined
orthologous variants: 144230570-G-A

70081238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144229694-T-C

70081680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144229089-A-G

70082764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144228629-C-T

70083333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144227631-A-G

70083411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144227555-C-T

http://identifiers.org/hco/11/GRCh38#70083529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144227491-C-A

70083801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144227295-C-T

70084070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144227081-G-T

70084241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144226860-A-G

70084432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144226672-G-C

70084615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144226598-G-C

70085093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144226221-A-G

70085146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144226101-T-C

70085281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144225884-A-G

http://identifiers.org/hco/11/GRCh38#70085290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144225877-C-A

70085290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron variant
orthologous variants: 144225877-C-T

70085499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 144225625-C-T

70087776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144223386-C-G

70087779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144223383-G-T

70087980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144223182-G-A

70087980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144223182-G-C

70087980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144223182-G-T

70088065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144223097-A-G

70088065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144223097-A-T

70088094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144223070-T-C

70088140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144223039-G-A

70088140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144223039-G-C

70088140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144223039-G-T

70088159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144223018-T-C

70088159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144223018-T-G

http://identifiers.org/hco/11/GRCh38#70088228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144222985-C-A

70088228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144222985-C-G

70088228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144222985-C-T

70090587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144221336-A-G

70090646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144221260-T-C

70090753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144221123-T-G

70092238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144218640-C-T

70093004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217945-T-G

70093214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217805-T-A

70093214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217805-T-C

70093223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217796-T-C

70093480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217574-G-A

70093483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217571-C-T

70093545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217510-T-C

70093550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217505-C-T

70094293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144217081-A-G

70094446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144216960-G-A

70095742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144215984-G-A

70096344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144215483-C-T

70097460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144214740-C-G

70097756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144214447-C-T

70097757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144214446-G-A

70098974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144213640-C-G

70099009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144213614-G-A

70099281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144213364-C-T

70099379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144213275-G-A

http://identifiers.org/hco/11/GRCh38#70100000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144212704-C-A

70102665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144211164-A-T

http://identifiers.org/hco/11/GRCh38#70102962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144210929-C-A

70102962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144210929-C-T

70102996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144210912-G-A

70102996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144210912-G-T

70103174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144210740-G-A

70103174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144210740-G-T

70103382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144210455-T-A

70103678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144210170-C-T

70103764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144210093-C-G

70103764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144210093-C-T

70104017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144209467-A-G

http://identifiers.org/hco/11/GRCh38#70104092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144209392-C-A

70104092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144209392-C-T

70104674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144208905-G-A

70104694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144208882-G-A

70104797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144208795-G-A

70104880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144208735-C-G

70104888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144208725-G-A

70105045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144208646-G-A

70105053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144208638-G-A

70105150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144208606-T-C

http://identifiers.org/hco/11/GRCh38#70105618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144208091-C-A

70105618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144208091-C-G

70105618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144208091-C-T

70105643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144208068-T-C

70106374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144207403-T-C

70106931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144205846-G-A

70106962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144205815-G-A

70107015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144205723-T-A

70107054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144205665-T-G

70107055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144205664-G-T

70107205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144205433-A-T

http://identifiers.org/hco/11/GRCh38#70107651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144204873-C-A

70108022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144204579-G-A

70108022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144204579-G-T

70108233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144204367-G-A

70108233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144204367-G-T

http://identifiers.org/hco/11/GRCh38#70108274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144204345-C-A

70108274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144204345-C-T

70110652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144202831-C-T

70110753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144202737-A-G

70110826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144202655-A-G

70110837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144202644-A-G

70110891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144202598-G-T

70111149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 144202352-G-T

70111442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144202070-G-A

70111624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144201896-T-C

http://identifiers.org/hco/11/GRCh38#70111811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#144201709-A-C

70111811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144201709-A-G

70111811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144201709-A-T

70111842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144201680-G-A

70111842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144201680-G-T

70111872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144201650-T-A

70112162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144201417-G-A

70112253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144201330-G-A

70112408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144201191-G-T

70113550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144200579-T-G

70113663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144200512-T-A

70114470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144199758-G-A

70115055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144199284-A-G

70116106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144198728-A-G

70116260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144198578-A-G

70116300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144198540-T-A

http://identifiers.org/hco/11/GRCh38#70116315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144198526-C-A

70116315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144198526-C-T

70116423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144198517-A-G

70116440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144198500-T-C

70116522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144198419-G-A

70116522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144198419-G-T

70116924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144198139-A-G

70117185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144198004-C-T

70118138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144197387-T-C

70118418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144197160-T-C

70118418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144197160-T-G

70118498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144197059-T-C

70118524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144197036-A-T

70118539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144197021-G-T

70118632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196922-A-G

70118670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196883-G-A

70118675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196878-G-A

70118675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196878-G-C

70118675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196878-G-T

70118706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196844-T-A

70118706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196844-T-G

70118707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196843-T-A

70118707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196843-T-G

70118717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196833-G-C

70118742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196808-T-C

70118756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196794-G-T

70120219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144196237-A-T

70120475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144195984-C-T

70120517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144195942-G-T

70124248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144192564-A-G

http://identifiers.org/hco/11/GRCh38#70124282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144192487-C-A

70124282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144192487-C-T

70124289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144192459-T-C

70124306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144192345-G-A

70124306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144192345-G-C

70124344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144192305-C-T

70124490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144192145-A-G

70124775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144191888-C-T

70124995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144191661-G-A

70125028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144191629-G-A

70125071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144191589-G-A

70125148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144191525-G-T

http://identifiers.org/hco/11/GRCh38#70125494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144191396-C-A

70125494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144191396-C-G

70125845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144191138-A-T

http://identifiers.org/hco/11/GRCh38#70125905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144191083-C-A

70125905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144191083-C-T

70128329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144190160-G-A

70128386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144190104-G-A

70128911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144189635-G-T

70129013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144189524-T-C

70129077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144189455-G-A

70129271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144189330-G-A

70129271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144189330-G-T

70129306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144189298-G-A

70129306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144189298-G-C

http://identifiers.org/hco/11/GRCh38#70129363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144189244-C-A

http://identifiers.org/hco/11/GRCh38#70129395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144189223-C-A

70129561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144189157-A-G

70130002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144188937-G-A

70130232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144188722-A-G

70130237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144188719-C-T

70130483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144188497-C-G

70130515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144188451-G-A

70130515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144188451-G-T

70130776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144188243-C-G

70130799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144188219-A-G

70130800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144188218-G-A

http://identifiers.org/hco/11/GRCh38#70130864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144188172-C-A

70130864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144188172-C-T

70131081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144187959-C-T

70131610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144187721-G-A

70131900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144187509-G-A

70131900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144187509-G-T

70134955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144185013-C-G

70141622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144182132-G-T

70141916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144181897-C-G

70141926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144181882-G-A

http://identifiers.org/hco/11/GRCh38#70149832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144175376-C-A

70149832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144175376-C-G

70149832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144175376-C-T

70149873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144175341-A-G

http://identifiers.org/hco/11/GRCh38#70149891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144175323-C-A

70149891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144175323-C-T

70150161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144175110-G-T

70150224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144175080-T-C

70150292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144175012-G-A

70150661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144174617-A-G

70151182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144173956-C-T

70151242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144173892-C-T

70151585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144173630-A-G

70151658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144173557-A-T

70151699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144173516-C-T

70151731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144173483-T-C

70152518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144173152-G-A

70152518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144173152-G-C

70152537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144173132-T-C

70152655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144173028-T-C

70152708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144172975-T-G

70153036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144172676-T-A

70153145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144172553-G-A

70153145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144172553-G-T

http://identifiers.org/hco/11/GRCh38#70153237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144172303-C-A

70153237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144172303-C-T

70153372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144172179-G-A

70153597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144171970-G-C

http://identifiers.org/hco/11/GRCh38#70154749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144171524-C-A

70154749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144171524-C-T

http://identifiers.org/hco/11/GRCh38#70155605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144169984-C-A

70155651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144169947-G-A

http://identifiers.org/hco/11/GRCh38#70156042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144169578-A-C

70156042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144169578-A-G

70156084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144169538-T-A

70156123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144169500-G-A

70156123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144169500-G-C

70156123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144169500-G-T

http://identifiers.org/hco/11/GRCh38#70156135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144169488-C-A

70156135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144169488-C-T

70156196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144169440-G-A

70156270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144169370-T-C

70156486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144169069-C-T

70156496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144169059-T-C

70156583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144168967-C-T

70156742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144168805-G-C

http://identifiers.org/hco/11/GRCh38#70156878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144168705-C-A

70156878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144168705-C-T

http://identifiers.org/hco/11/GRCh38#70156947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144168659-A-C

70156947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 144168659-A-G

70157058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144168520-G-A

70157075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144168503-G-T

http://identifiers.org/hco/11/GRCh38#70157277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144168253-C-A

70159097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144167347-G-T

70159252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144167225-G-A

70159411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144167086-G-A

70159440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144167052-A-G

70159448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144167044-G-A

70159784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144166777-G-C

70161115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144165615-G-T

70161145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144165566-C-T

70161242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144165469-C-T

70161398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144165310-T-A

http://identifiers.org/hco/11/GRCh38#70161458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144165262-C-A

70161600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144165200-A-G

70161786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144165020-G-A

70161786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144165020-G-T

http://identifiers.org/hco/11/GRCh38#70161789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144165017-C-A

70161789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144165017-C-G

http://identifiers.org/hco/11/GRCh38#70161797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144164997-C-A

70161811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144164984-G-A

70161819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144164976-G-A

70161906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144164902-G-A

70163180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144164730-C-T

http://identifiers.org/hco/11/GRCh38#70163203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144164709-C-A

70163206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144164706-A-G

70163319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144164599-C-T

http://identifiers.org/hco/11/GRCh38#70165349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144162782-C-A

70165349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144162782-C-T

70165402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144162735-T-A

http://identifiers.org/hco/11/GRCh38#70165403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144162734-C-A

70165420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144162732-C-T

70165437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144162715-T-A

70165437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144162715-T-C

70165446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144162705-G-A

70165446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144162705-G-T

70165597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144162557-G-A

http://identifiers.org/hco/11/GRCh38#70165697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144162454-A-C

70165697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144162454-A-G

70165712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144162439-A-G

70167103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161912-G-A

70167103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161912-G-T

http://identifiers.org/hco/11/GRCh38#70167111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144161900-C-A

70167111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161900-C-T

70167112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161899-A-T

http://identifiers.org/hco/11/GRCh38#70167113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144161898-C-A

70167164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161863-A-T

70167177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161853-T-A

70167177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161853-T-G

70167296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144161744-C-G

70167306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144161734-T-C

70167333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144161707-G-A

http://identifiers.org/hco/11/GRCh38#70167427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144161164-A-C

70167427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161164-A-G

70167427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161164-A-T

http://identifiers.org/hco/11/GRCh38#70167442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144161152-C-A

70167442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161152-C-G

70167442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161152-C-T

http://identifiers.org/hco/11/GRCh38#70167495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144161095-C-A

70167495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161095-C-T

http://identifiers.org/hco/11/GRCh38#70167507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144161083-C-A

70167507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161083-C-T

http://identifiers.org/hco/11/GRCh38#70167518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144161072-A-C

70167518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161072-A-G

70167527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161063-G-A

70167527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161063-G-T

70167558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144161022-C-T

70167747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144160924-G-A

70167747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144160924-G-T

70167850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144160848-A-G

70168128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144160614-G-A

70168136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144160606-C-T

70168137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144160605-G-A

70168158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144160584-G-A

70168204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144160545-G-T

70168245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144160505-C-T

70168263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144160483-C-T

http://identifiers.org/hco/11/GRCh38#70168596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144160072-A-C

70168627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144160041-C-T

70169051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144159683-G-A

70169052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144159682-G-A

http://identifiers.org/hco/11/GRCh38#70169127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144159602-C-A

70169248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144159496-G-A

70169418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144159330-A-G

70169566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144159028-A-G

70169973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144158587-C-T

70169997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144158572-G-A

70170053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144158530-G-A

http://identifiers.org/hco/11/GRCh38#70170071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144158514-C-A

70170071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144158514-C-T

http://identifiers.org/hco/11/GRCh38#70170137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144158451-A-C

70170137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144158451-A-G

http://identifiers.org/hco/11/GRCh38#70170169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144158421-C-A

70170169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 144158421-C-T

http://identifiers.org/hco/11/GRCh38#70170176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144158414-C-A

70170176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144158414-C-T

http://identifiers.org/hco/11/GRCh38#70170207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144158391-C-A

70170207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144158391-C-T

http://identifiers.org/hco/11/GRCh38#70170243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144158379-C-A

70170294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144158340-T-A

70170294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144158340-T-G

http://identifiers.org/hco/11/GRCh38#70170301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144158333-A-C

70170301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144158333-A-G

70170301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144158333-A-T

70170739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144157588-A-G

70170750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144157538-G-A

70170764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144157521-A-T

70170823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144157464-G-A

70170823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144157464-G-C

70170823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144157464-G-T

70170919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144157296-G-A

70170919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144157296-G-C

70170919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144157296-G-T

http://identifiers.org/hco/11/GRCh38#70171062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144157161-A-C

http://identifiers.org/hco/11/GRCh38#70171067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144157157-C-A

70171067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144157157-C-T

70171075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144157149-A-G

70171120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144157120-A-G

70171192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144157068-G-T

http://identifiers.org/hco/11/GRCh38#70171195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144157065-A-C

70171195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144157065-A-G

70171220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144157040-C-T

70171528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144156321-C-T

70175502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154168-C-T

70175675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154010-G-A

70175699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153985-G-A

http://identifiers.org/hco/11/GRCh38#70181107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#144150368-A-C

70181107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144150368-A-G

70181162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144150316-G-A

70181211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144150279-A-G

70181212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144150278-C-T

70181277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144150228-A-G

70181409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144150125-A-G

70181409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144150125-A-T

70181578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144149986-G-A

70181580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144149984-T-C

70181970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144149780-C-T

70182340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144149440-T-A

70182467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144149388-T-C

http://identifiers.org/hco/11/GRCh38#70182690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144149173-C-A

70182754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144149109-A-G

70182933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144148974-A-G

70183540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144148286-G-A

70183985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147889-T-C

70184070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147822-G-A

70184082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147811-G-A

70185819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144146326-G-A

70185819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144146326-G-C

70185819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144146326-G-T

http://identifiers.org/hco/11/GRCh38#70185820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144146325-A-C

70185820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144146325-A-G

http://identifiers.org/hco/11/GRCh38#70187688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144144049-C-A

70187688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144144049-C-G

70187688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144144049-C-T

70187996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143742-G-A

70187996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143742-G-C

70187996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143742-G-T

70188051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144143684-G-A

70188051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144143684-G-T

70188087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144143646-A-G

70188141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143595-T-C

http://identifiers.org/hco/11/GRCh38#70188331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144143422-A-C

70188331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143422-A-G

70188341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143413-G-A

70188341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143413-G-C

70188341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143413-G-T

70188621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143157-A-G

70188637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143144-G-T

70188671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143119-T-C

70188692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143098-C-T

70188772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143041-G-T

70189166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144142676-C-G

http://identifiers.org/hco/11/GRCh38#70189228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#144142617-A-C

70189261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144142575-A-T