47285900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904828-G-T

47285919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904809-A-G

47285976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904763-C-T

47285992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904747-G-A

http://identifiers.org/hco/18/GRCh38#47285994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76904745-C-A

47287765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904383-T-C

47287918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904272-A-G

47288105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904104-G-A

47288157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904051-G-A

47288176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904032-G-A

47288482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76903727-T-C

http://identifiers.org/hco/18/GRCh38#47289030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76902909-C-A

47289030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76902909-C-G

47289076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76902869-A-G

47289599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76902271-C-T

47289633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76902238-A-G

47289654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76902218-C-T

47289695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76902178-G-A

http://identifiers.org/hco/18/GRCh38#47289870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76901982-A-C

47290032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76901810-T-C

47290057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76901767-G-T

47290080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76901743-G-A

47290109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76901714-C-G

47290123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76901700-T-G

47292702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76899250-G-C

47292772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76899045-C-T

47293189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76898323-A-T

47293376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76898130-C-T

47293541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76897958-G-A

47293541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76897958-G-T

47293587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76897908-T-A

47293624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76897873-G-A

47293697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76897807-T-G

47294068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76897429-G-A

47294106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76897392-A-G

47294184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76897315-C-T

47301362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890293-G-A

47301362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890293-G-C

47301459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890179-T-C

47301565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890095-C-T

47301613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76890029-A-G

47301651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889997-T-A

47301651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889997-T-C

47301816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889861-C-T

47302062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889638-G-A

47302214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889574-G-A

47302310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889527-A-T

http://identifiers.org/hco/18/GRCh38#47302395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76889466-C-A

47302435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889432-C-T

47302737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889139-T-A

47302796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889077-T-C

47302796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889077-T-G

47302810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889063-G-A

47302810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889063-G-T

http://identifiers.org/hco/18/GRCh38#47302838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76889058-C-A

47302842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889054-T-A

47302842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889054-T-C

47302842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889054-T-G

47302877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889018-T-C

47302901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76888993-A-T

47302933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76888960-C-T

47302982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76888913-C-T

47303872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76881894-C-G

47303912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76881854-G-T

47304060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76881692-C-T

47304792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76881082-G-A

http://identifiers.org/hco/18/GRCh38#47304811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76881062-C-A

47304811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76881062-C-T

47304818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76881054-A-G

http://identifiers.org/hco/18/GRCh38#47304994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76880928-C-A

47305091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76880872-A-G

47305127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76880836-T-C

47305432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76880572-A-G

47305432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76880572-A-T

47305448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76880556-T-G

47305470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76880535-A-G

47305578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76880428-A-G

47306427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76873852-C-T

http://identifiers.org/hco/18/GRCh38#47306714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76873562-A-C

47306759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76873523-G-A

47306787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76873495-C-T

47306794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76873488-C-G

http://identifiers.org/hco/18/GRCh38#47306835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76873421-A-C

47306835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76873421-A-T

47307053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76873215-T-C

47307157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76873092-G-A

47307260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76873002-G-C

47307324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76872935-T-C

47307615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76872679-A-T

47307855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76872469-G-T

47309707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76869659-G-T

http://identifiers.org/hco/18/GRCh38#47309780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76869590-C-A

47309870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76869528-C-G

47309942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76869469-A-G

47310357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76869093-G-T

47311504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76868138-C-T

47312002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76867647-T-C

47312002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76867647-T-G

47312132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76867548-T-C

47312220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76867452-T-C

47312422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76867251-T-C

47312582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76867105-T-C

47312623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76867067-A-G

47312692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76867007-G-A

http://identifiers.org/hco/18/GRCh38#47312807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76866893-C-A

47313004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76866719-G-A

47313009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76866712-T-A

47313009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76866712-T-C

47313086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76866655-T-C

47314121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76865191-C-T

47314178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76865137-C-T

47315141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76862099-T-C

http://identifiers.org/hco/18/GRCh38#47315144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76862096-A-C

47315353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76861906-T-C

47315766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76861507-A-G

47315766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76861507-A-T

47315858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76861431-A-G

47315907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76861382-T-C

47315926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76861366-G-C

47316190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76861101-G-A

47316252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76861037-G-C

47316321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76860979-G-A

47316634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76860702-G-A

47316634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76860702-G-T

47316653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76860659-C-T

47317289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76860340-C-G

47317289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76860340-C-T

http://identifiers.org/hco/18/GRCh38#47317682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76860043-A-C

47317705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76860020-T-C

47317858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76859823-C-T

47318019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76859626-T-C

47319243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76859465-A-G

47319382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76859376-T-C

47319556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76859206-G-C

http://identifiers.org/hco/18/GRCh38#47319844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76858918-C-A

47319844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76858918-C-T

47319979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76858782-G-A

47320844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76856383-G-A

47321003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76856246-T-C

47321412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76855884-G-A

47321412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76855884-G-C

47321473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76855823-C-G

47321982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76855316-C-G

47322058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76855243-G-A

47322403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76854843-A-G

47322574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76854709-A-G

http://identifiers.org/hco/18/GRCh38#47326330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76854132-C-A

47326368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76854093-G-A

47326380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76854081-G-A

47326443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76854018-A-G

47326955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76853598-T-G

47326968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76853588-C-T

47327019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76853572-T-G

47327066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76853546-A-G

47327221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76853388-G-A

47327587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76853083-C-T

47327599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76853075-C-T

47327631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76853043-T-A

47327647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76853027-T-C

47327663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76853011-C-G

47327706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76852994-T-C

http://identifiers.org/hco/18/GRCh38#47327874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76852840-C-A

47327874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76852840-C-G

47327874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76852840-C-T

47327906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76852102-C-T

47328157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76851910-T-C

47328210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76851855-T-C

47328306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76851762-C-T

http://identifiers.org/hco/18/GRCh38#47328497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76851589-C-A

47328529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76851557-T-C

47328632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76851464-G-C

47328761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76851335-A-G

47330636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76850983-T-C

http://identifiers.org/hco/18/GRCh38#47330673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76850974-C-A

47330706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76850941-C-T

47330830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76850813-A-G

47330862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76850764-C-G

47330862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76850764-C-T

47330863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76850763-C-G

47330863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76850763-C-T

47331275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76850374-G-A

47331521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76850124-A-G

47331590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76850066-C-G

47331590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76850066-C-T

http://identifiers.org/hco/18/GRCh38#47332242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76849448-C-A

47332269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76849421-C-T

47332299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76849401-A-G

47332489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76849275-G-T

47332511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76849253-C-T

47332967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76849046-G-A

47333522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76848705-C-T

47333591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76848635-A-G

47333709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76848512-C-T

47333726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76848495-G-A

47333731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76848490-T-C

47334534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76847728-T-G

http://identifiers.org/hco/18/GRCh38#47334785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76847492-A-C

47334835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76847445-A-G

47335000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76847281-G-C

47335086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76847200-C-T

47335123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76847163-G-A

47335123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76847163-G-C

47335123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76847163-G-T

47335187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76847105-A-G

47335217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76847076-A-G

47335422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76846895-T-C

47335490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76846823-A-G

47335542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76846767-G-A

47335587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76846734-C-T

47335677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76846656-G-A

47335744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76846418-C-T

47336021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76846037-T-C

47336340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76845859-G-A

47336589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76845671-C-T

47336841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76845473-A-G

47336935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76845407-T-G

47337651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844707-G-A

47337680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844677-G-A

47337777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844587-A-G

47337783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844581-G-C

47337788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844576-C-T

47337797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844567-G-A

47337808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844551-G-A

47337854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844501-T-C

47337897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844453-T-C

47337939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844411-G-A

47337947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844406-T-C

47338228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844094-T-C

47338257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844062-A-T

47338267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76844052-G-C

http://identifiers.org/hco/18/GRCh38#47338649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76843684-C-A

47338743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76843594-T-C

47338876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76843460-A-T

47339855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76842594-T-C

47339856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76842593-T-C

47339951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76842493-G-A

47340073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76842388-G-T

47340350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76842118-T-C

47340762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76841699-A-G

47340787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76841676-G-T

47340803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76841660-A-G

47340870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76841593-G-A

47341346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76841466-C-T

47341461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76841341-A-G

47341469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76841333-C-G

47341592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76841235-G-A

47341973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76840854-T-C

47342129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76840696-A-G

47342253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76840573-T-C

47343666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76840048-C-T

47343696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76840017-C-T

47343728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76839985-C-T

http://identifiers.org/hco/18/GRCh38#47344015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76839734-C-A

47344015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76839734-C-T

47344343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76839455-T-C

47344374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76839424-G-T

http://identifiers.org/hco/18/GRCh38#47345456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76839392-A-C

47345456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76839392-A-G

47345462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76839387-T-C

47345550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76839299-G-T

47345641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76839221-C-T

47345654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76839208-C-T

47345816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76839063-C-T

47345839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76839039-A-G

47345863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76839025-A-G

47345917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76838979-A-G

47345917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76838979-A-T

http://identifiers.org/hco/18/GRCh38#47346308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76838569-A-C

47346320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76838557-T-C

47346360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76838517-T-C

47346379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76838499-G-A

47346379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76838499-G-C

47346409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76838469-G-T

47346505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76838373-T-G

47346642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76838197-T-A

47346718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76838131-T-C

47346747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76838104-G-A

47346798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76838054-A-G

47346930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76837925-C-T

47346968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76837887-T-C

http://identifiers.org/hco/18/GRCh38#47346993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76837863-C-A

47346993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76837863-C-T

47347000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76837856-G-C

47347478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76837794-T-C

http://identifiers.org/hco/18/GRCh38#47347501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76837771-C-A

47347537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76837736-A-G

47347577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76837697-C-T

47347582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76837692-G-A

47347848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76837436-T-C

47347883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76837402-T-C

http://identifiers.org/hco/18/GRCh38#47348161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76837205-C-A

47348161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76837205-C-T

47354904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76836242-C-T

47354926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76836220-T-C

47355728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76834327-T-C

47355750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76834305-C-T

47355762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76834293-G-A

47356044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76834021-G-A

http://identifiers.org/hco/18/GRCh38#47356080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76833985-C-A

http://identifiers.org/hco/18/GRCh38#47356150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76833920-C-A

47356150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833920-C-T

http://identifiers.org/hco/18/GRCh38#47356153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76833917-C-A

47356153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833917-C-T

47356258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833832-T-C

47356283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833812-G-T

47356295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833800-C-G

47356593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833538-T-G

47356603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833528-G-A

47356609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833522-G-A

47356641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833493-C-T

47356698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833436-G-A

47356699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833435-C-G

47356807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833330-T-C

47357108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833028-A-G

47357123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76833015-C-G

47357149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76832988-A-G

47357311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76832836-G-A

47357372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76832775-A-G

47357389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76832758-G-A

47357389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76832758-G-C

47357639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76832371-T-G

47358085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76830788-A-G

47372123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76827554-T-C

47372394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76827297-T-C

47372454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76827249-C-G

47372454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76827249-C-T

47372497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76827206-T-G

47372593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76827115-A-G

47372652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76827068-A-G

47372657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76827063-A-T

47372922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76826799-T-A

47374293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76824119-C-G

47374457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76823968-T-C

47374542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76823887-T-C

47374564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76823865-G-A

47374638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76823812-C-T

47374751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76823705-C-T

47375037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76823262-A-T

47375064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76823246-T-C

47375262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76822878-A-G

47375275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76822865-A-G

47375352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76822793-C-T

47375611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76822587-G-A

47376552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76822045-G-C

47376636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76821998-C-T

47376938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76821753-A-G

47376965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76821679-G-C

http://identifiers.org/hco/18/GRCh38#47377548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76821543-A-C

47377556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76821535-G-A

http://identifiers.org/hco/18/GRCh38#47377650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76821441-C-A

47377708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76821394-C-T

47377853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76821269-T-C

47377928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76821204-C-G

47377974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76821155-C-G

47378020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76821108-G-A

47378020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76821108-G-C

47378035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76821093-C-T

47378489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76820668-C-T

47378540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76820613-G-A

47378721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76820457-C-G

47378905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76820332-G-C

47378950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76820300-C-T

47378953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76820297-C-T

http://identifiers.org/hco/18/GRCh38#47379029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76820223-C-A

http://identifiers.org/hco/18/GRCh38#47379031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76820221-C-A

47380595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819869-A-G

47380683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819781-A-G

47380724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819740-G-A

47380724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819740-G-C

47381043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819472-G-C

47381078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819431-G-A

47381192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819353-T-C

47381206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819339-T-C

47381232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819313-T-G

47381271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819274-G-A

47381327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819220-G-A

47381427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819149-A-G

47381461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819120-G-C

47381462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819119-G-A

47381680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818923-T-C

47381680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818923-T-G

47381789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818834-C-T

47381867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818756-C-T

47382198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818451-C-T

47382224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818427-G-A

47382401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818251-C-T

47382509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818155-G-A

47382811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76817991-G-A

47382971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76817835-A-G

47383038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76817775-A-G

47389322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76817544-A-G

47389795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76816742-A-G

47390704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76815918-A-G

47390749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76815876-G-A

47391512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76815069-G-T

47392438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76814568-C-T

47392513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76814160-T-C

47392523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76814150-G-T

http://identifiers.org/hco/18/GRCh38#47392525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76814148-C-A

47392695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76813971-G-A

47392760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76813921-G-A

47392837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76813874-G-A

47392837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76813874-G-T

47392850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76813859-T-C

47392880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76813835-A-G

47394314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811979-A-G

47394316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811977-G-T

47394347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811946-G-A

http://identifiers.org/hco/18/GRCh38#47394489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76811807-A-C

47394507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811784-T-C

47394535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811756-T-C

47394646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811649-A-G

47394655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811641-T-C

47394820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811485-T-G

47394945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811322-A-G

47394945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811322-A-T

http://identifiers.org/hco/18/GRCh38#47394946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76811321-C-A

47395031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811234-G-A

47395041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811220-A-G

http://identifiers.org/hco/18/GRCh38#47395047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76811214-A-C

47395047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811214-A-G

47395047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811214-A-T

47395050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811211-C-T

47395087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811175-A-G

47395087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811175-A-T

47395102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811160-G-A

47395247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76811013-C-T

47395299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76810965-A-G

47395326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76810945-T-C

47395349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76810922-T-A

47395351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76810920-G-A

47395364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76810910-G-C

47395370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76810904-G-C

47396544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76810672-C-G

47397277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76808306-C-T

http://identifiers.org/hco/18/GRCh38#47397766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76807441-A-C

47397773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76807434-A-T

47397789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76807418-C-T

47399071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76805866-A-G

http://identifiers.org/hco/18/GRCh38#47399498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76803469-A-C

47399498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76803469-A-G

47399588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76803413-G-C

http://identifiers.org/hco/18/GRCh38#47399591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76803410-C-A

47399591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76803410-C-T

http://identifiers.org/hco/18/GRCh38#47399626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76803377-A-C

47399727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76803285-A-G

47399880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76803170-G-C

47400002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76803054-G-A

47403039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76802685-G-T

47403134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76802597-C-T

47403475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76802240-T-C

47403768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76801958-C-T

47403812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76801915-C-G

47404191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76801553-C-G

47404191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76801553-C-T

47404196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76801548-T-A

47404257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76801493-C-G

47404257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76801493-C-T

47404360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76801418-G-A

47404438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76801343-A-G

47404463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76801318-G-C

47404522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76801255-G-A

47411134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76800102-G-A

47411588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76799650-A-G

47411630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76799612-C-T

47411810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76799431-A-G

http://identifiers.org/hco/18/GRCh38#47411829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76799405-C-A

47411990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76799293-G-A

47411990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76799293-G-T

47412002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76799283-G-A

47412006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76799279-G-T

47412051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76799165-A-G

47412135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76799080-G-A

47412260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76798949-C-T

47413468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76796952-A-G

http://identifiers.org/hco/18/GRCh38#47413536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76796877-C-A

47413688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76796722-A-G

47413692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76796718-C-T

47413827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76796598-G-A

47413884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76796540-T-C

http://identifiers.org/hco/18/GRCh38#47414328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76795208-A-C

47414396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76795135-T-G

47415658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76793900-A-G

47415677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76793882-A-G

http://identifiers.org/hco/18/GRCh38#47415756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76793807-A-C

47415756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76793807-A-G

47416276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76793220-T-A

47416558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76792965-T-A

47416842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76792691-T-G

47416926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76792609-T-A

47416926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76792609-T-C

47417085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76792303-T-C

47417111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76792277-C-G

47417304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76792107-G-T

47417463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76792005-A-G

http://identifiers.org/hco/18/GRCh38#47417466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76792002-C-A

47417471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76791998-T-G

47417594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76791916-G-T

47417731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76791806-G-A

http://identifiers.org/hco/18/GRCh38#47417781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76791760-A-C

47417829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76791728-G-A

47417848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76791711-C-T

47418042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76791544-T-C

47418103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76791491-A-G

47418103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76791491-A-T

47418748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76791121-T-A

47418929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790972-G-A

47419046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790839-G-T

47419716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790688-G-T

http://identifiers.org/hco/18/GRCh38#47419860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76790550-C-A

47419883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790527-G-A

47420061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790166-G-A

47420061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790166-G-C

47420089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790138-C-T

47420210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790019-C-T

47420250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76789980-G-T

47420340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76789893-C-T

47420792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76789379-G-C

47420952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76789227-T-C

47421116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76789065-T-C

47421141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76789042-G-A

47421229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76788959-T-A

47421258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76788930-G-A

http://identifiers.org/hco/18/GRCh38#47421314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76788874-C-A

47421369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76788832-C-T

47421393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76788808-A-T

47421716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76788477-C-G

47422035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76788107-G-T

47422094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76788053-T-G

47422843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76787423-A-G

47422843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76787423-A-T

47422913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76787352-T-C

47425369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76786078-G-A

47425674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785806-C-T

47426221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785345-G-A

http://identifiers.org/hco/18/GRCh38#47426267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76785296-C-A

47426407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785158-G-T

http://identifiers.org/hco/18/GRCh38#47426418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76785147-C-A

47426652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784986-G-A

47426686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784952-T-C

47427701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784587-G-A

47427727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784561-C-T

47427739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784549-T-C

47427775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784520-T-A

47428106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784191-T-C

47428120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784177-C-G

47428362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76783929-A-G

47428522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76783765-C-G

47429723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

47430008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

47430190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

47430210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

47430255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

47430255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

47430322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

47431730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76782264-T-C

47432140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781534-T-G

47432178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781495-A-G

47432480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781200-T-C

47432488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781192-G-A

47432488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781192-G-C

47432546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780617-G-A

47432546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780617-G-C

47432591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780573-C-T

47432703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780456-C-G

47432745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780407-G-A

47433051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780233-A-T

47433097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780182-G-T

47433123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780157-A-T

http://identifiers.org/hco/18/GRCh38#47433141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76780120-C-A

47433149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780112-G-A

47433149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780112-G-C

http://identifiers.org/hco/18/GRCh38#47433501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76779758-C-A

47433501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779758-C-T

47433512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779747-A-G

47433741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779202-T-C

47433758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779185-A-T

47433881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779036-G-A

47433904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779005-C-T

47434065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76778724-T-C

47434088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76778701-G-A

47434178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777979-A-T

47434246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777924-G-A

http://identifiers.org/hco/18/GRCh38#47434302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76777875-C-A

47434518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777666-A-G

47434789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777406-A-G

http://identifiers.org/hco/18/GRCh38#47434800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76777395-A-C

47434875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777341-G-T

47434960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777266-G-T

47434993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777233-A-T

47435240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777015-A-G

47435240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777015-A-T

47435503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776787-T-A

47435503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776787-T-C

47435604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776689-G-A

47435799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776498-G-A

47437530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776061-G-T

47437564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776029-G-T

47437942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76775598-C-T

47438308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76775247-C-G

47438411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76775168-C-T

47438454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76775127-G-C

47438553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76775032-C-T

47439122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774896-C-T

47439358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774685-C-T

47439378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774664-A-G

47439425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774612-A-G

47439483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774574-A-G

47439518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774541-G-T

47439948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774124-C-T

47440055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774035-A-G

47440068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774022-C-T

47440144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772427-A-G

47440186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772378-C-T

47440320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772268-A-T

47440346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772242-G-A

47440346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772242-G-C

47440394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772196-G-A

47440407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772183-C-G

47440532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772118-A-G

47440612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772078-G-A

http://identifiers.org/hco/18/GRCh38#47440640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76772053-A-C

47440760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771944-C-T

47440768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771936-T-C

47440782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771922-G-A

47440885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771684-A-G

47440927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771654-G-A

47440927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771654-G-C

47440927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771654-G-T

47441144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771470-G-T

47441145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771469-A-G

http://identifiers.org/hco/18/GRCh38#47441197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76771421-A-C

47441197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771421-A-G

47441312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771302-C-T

47441383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771246-T-A

47441383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771246-T-C

http://identifiers.org/hco/18/GRCh38#47442045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76770615-A-C

47442045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76770615-A-T

47442117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76770543-C-T

47442406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76770254-C-T

47442441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76770219-G-C

47442473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76770189-C-T

47442477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76770185-A-G

47442949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76769739-G-A

47443058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76769355-A-G

47443354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76769066-T-C

http://identifiers.org/hco/18/GRCh38#47443466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76768960-C-A

47443508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76768923-C-T

http://identifiers.org/hco/18/GRCh38#47448207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76766683-C-A

47448389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76766501-G-A

47448769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76766130-G-A

http://identifiers.org/hco/18/GRCh38#47448819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76766075-A-C

47448819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76766075-A-G

47448854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76766040-C-T

47448904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76765991-A-G

47448920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76765975-T-C

47449130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76765768-G-C

47449220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76765680-C-T

47449317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76765589-A-G

47449325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76765583-G-A

http://identifiers.org/hco/18/GRCh38#47449817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76764174-A-C

47449817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76764174-A-G

47449889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76764102-A-T

47449916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76764076-G-T

47450069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763685-C-G

http://identifiers.org/hco/18/GRCh38#47450182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76763575-C-A

47450234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763520-A-G

47450434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76762865-C-T

47450508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76762788-C-G

47451240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76762427-G-T

47451298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76762378-G-A

http://identifiers.org/hco/18/GRCh38#47451551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76762025-A-C

47451579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761998-A-G

47451701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761893-G-A

47451701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761893-G-T

47451734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761864-A-T

http://identifiers.org/hco/18/GRCh38#47451945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76761679-A-C

47451945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761679-A-G

47452215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761455-G-A

47453834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761274-A-G

47453905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761201-C-T

47453915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761191-G-A

47453918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761188-G-A

47454018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761095-A-G

47454062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761050-G-A

47454110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761036-C-G

47454198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760954-G-A

47454205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760947-C-G

47454237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760915-G-T

47454347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760821-G-A

47455042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760588-C-G

47455042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760588-C-T

47455103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760520-G-A

47455164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760488-G-C

47455277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760391-A-G

47455487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760217-A-G

47455657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760059-C-T

47455660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760056-C-G

47456463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76759690-T-G

47456578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76759581-G-A

47456928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76759238-A-G

47457029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76759137-A-T

47457256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76758919-T-C

47457309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76758873-T-G

47457333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76758834-G-A

47457457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76758710-G-A

47457551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76758608-T-C

47457571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76758590-T-G

47457604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76758570-G-A

47457626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76758548-A-G

http://identifiers.org/hco/18/GRCh38#47458007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76758111-C-A

47458245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76757860-G-A

47458335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76757769-T-C

47458370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76757736-C-T

47458421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76757687-G-A

47458432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76757675-G-C

47458511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76757589-G-C

47459078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76757453-C-T

47459187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76757356-C-G

47459307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76757224-G-A

47459761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76756514-G-A

47459761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76756514-G-C

47462281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76755716-G-A

47462385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76755618-G-A

47462757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76755104-G-C

47462853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76755035-G-T

http://identifiers.org/hco/18/GRCh38#47462941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76754875-C-A

47463070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754741-T-C

47463305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754505-G-T

47463407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754405-G-A

47463450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754361-T-G

47463465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754346-C-T

47463654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754146-G-A

47463816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76753034-C-T

47463817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76753033-A-G

http://identifiers.org/hco/18/GRCh38#47463984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76752913-A-C

47463984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752913-A-T

47464129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752766-G-A

47464129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752766-G-T

http://identifiers.org/hco/18/GRCh38#47464139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76752756-A-C

47464140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752755-T-A

47464213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752694-A-G

47464294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752628-T-A

http://identifiers.org/hco/18/GRCh38#47464314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76752606-C-A

47464364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752573-T-C

47464487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752223-G-A

47464539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752171-G-T

http://identifiers.org/hco/18/GRCh38#47464721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76752009-A-C

47469113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76750404-C-T

47469369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76750179-T-C

47469506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76750064-G-A

47469574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76749991-A-G

47469991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76749564-A-T

47470707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748964-G-C

47470707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748964-G-T

47470738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748933-T-C

47470772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748900-G-T

47470809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748862-A-T

47470858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748786-G-A

http://identifiers.org/hco/18/GRCh38#47470935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76748646-C-A

47470944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748637-G-A

47470998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748575-A-G

47471021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748552-C-T

47471817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748406-G-T

47471903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748339-A-G

47471903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748339-A-T

47471929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748322-T-C

47471929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748322-T-G

47471960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748295-G-A

47472002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748251-G-A

47472134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748133-T-C

47472329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747944-C-T

47472385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747885-G-A

47472750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747730-T-A

47472756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747724-T-A

47472756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747724-T-C

47472858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747626-G-A

47472901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747583-C-G

http://identifiers.org/hco/18/GRCh38#47472914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76747570-C-A

47472953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747532-C-T

47472954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747531-G-A

47472954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747531-G-C

47474321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76746429-T-C

47474339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76746411-C-G

47474425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76746304-A-G

47474798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76745934-C-T

47474906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76745834-A-G

47475451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76742839-G-A

47475613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76742681-C-G

47475738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76742528-A-G

http://identifiers.org/hco/18/GRCh38#47475832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76742438-C-A

47475832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76742438-C-T

47476066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76742241-C-G

47476309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76742076-A-G

47476844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76740074-T-A

47476855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76740063-G-C

http://identifiers.org/hco/18/GRCh38#47476930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76739990-C-A

47476930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76739990-C-G

47476930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76739990-C-T

47476936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76739984-T-C

47477374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76739283-A-G

http://identifiers.org/hco/18/GRCh38#47477503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76739103-C-A

47477940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76738710-A-G

47478111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76738533-T-C

47478218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76738427-G-A

47478252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76738393-G-T

47478397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76738252-A-G

47478526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76738125-A-T

47478909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737745-C-T

47479171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737488-T-C

47479363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737364-C-G

47479494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737241-T-C

47479666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737035-T-C

47480026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736728-C-T

47480034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736720-G-T

47480037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736717-C-T

47480175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736546-T-C

http://identifiers.org/hco/18/GRCh38#47480201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76736524-A-C

47480341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736395-T-C

47480341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736395-T-G

47480562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736133-C-T

47480688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76735987-A-T

47480690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76735985-T-A

47480765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76735908-T-A

47480865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76735788-A-G

47481131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76735457-C-T

47481616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76734610-G-C

47481866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76734355-C-G

47481877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76734344-C-T

47482087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76734167-C-T

47482147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76734128-C-T

47482152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76734123-A-G

47482255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76734006-C-G

47482290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76733971-G-T

47482304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76733957-A-G

47482312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76733949-G-T

47482363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76733892-C-G

47483200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76732631-T-C

47483925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76731970-C-T

47484176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76731736-C-T

47484982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730943-T-C

47485084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730840-C-T

47485106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730819-T-A

47485106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730819-T-C

47485159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730768-T-G

47485198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730732-C-T

47485261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730659-G-A

47485298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730624-G-A

47485303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730619-A-T

47487232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730396-C-T

47487295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730334-T-A

47487299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730330-C-T

47487456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730217-T-C

47487464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730208-G-A

47487627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730081-G-C

47487653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76730057-T-G

47487943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76729400-G-C

47488995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76728420-G-A

47488995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76728420-G-C

47489054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76728369-T-C

47489137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76728288-G-A

47489146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76728279-C-T

47489203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76728227-G-T

47489484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76727942-G-A

47489484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76727942-G-C

47489576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76727849-G-T

http://identifiers.org/hco/18/GRCh38#47489720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76727705-C-A

47489776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76727650-G-A

47489790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76727636-C-T

47489841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76727587-C-T

http://identifiers.org/hco/18/GRCh38#47490013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76727444-A-C

47490052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76727406-G-T

47490065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76727395-G-C

47490067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76727393-G-A

47490086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76727374-T-G

47490090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76727370-G-T

47490174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76727106-C-T

47490298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76726998-T-G

47490351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76726967-T-A

47490361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76726958-C-T

47490456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76726878-T-A

http://identifiers.org/hco/18/GRCh38#47490591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76726753-C-A

http://identifiers.org/hco/18/GRCh38#47493981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76722649-C-A

47494043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76722589-T-C

47494085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76722549-G-A

47494085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76722549-G-C

47494085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76722549-G-T

http://identifiers.org/hco/18/GRCh38#47494096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76722538-A-C

47494098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76722536-C-G

47494482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76722129-G-C

47494570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76722036-G-A

47494570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76722036-G-C

47494605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76721996-A-G

47494656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76721945-T-C

http://identifiers.org/hco/18/GRCh38#47494821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76721324-C-A

http://identifiers.org/hco/18/GRCh38#47494823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76721322-A-C

47494903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76721250-G-C

47494914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76721239-T-C

47494937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76721216-A-G

47495033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76721121-C-T

http://identifiers.org/hco/18/GRCh38#47495080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76721081-A-C

47495084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76721077-A-G

47495346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76720741-A-G

47495402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76720686-G-T

47495414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76720671-T-C

47495433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76720652-A-T

47495463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76720622-T-C

http://identifiers.org/hco/18/GRCh38#47495539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76720551-C-A

47495539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76720551-C-T

http://identifiers.org/hco/18/GRCh38#47495575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76720516-C-A

47495577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76720514-A-G

http://identifiers.org/hco/18/GRCh38#47496068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76720366-C-A

47496459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76719973-A-G

47496503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76719847-C-T

47496630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76719481-T-G

47496686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76719435-G-A

47496786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76719342-C-T

47496789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76719339-T-A

47497404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76717501-C-T

47497424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76717482-G-A

47497496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76717424-A-G

47499632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76714345-G-A

47499660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76714318-C-T

47499891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76714089-T-A

http://identifiers.org/hco/18/GRCh38#47500089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76713893-C-A

47500126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76713778-G-A

47500161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76713743-C-T

http://identifiers.org/hco/18/GRCh38#47500186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76713729-C-A

47500186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76713729-C-T

47500558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76713395-G-A

47500558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76713395-G-C

47500570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76713383-A-G

47501357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76713270-G-A

47501364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76713263-T-C

47501376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76713255-T-C

47501378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76713253-T-C

http://identifiers.org/hco/18/GRCh38#47501387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76713244-C-A

47501387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76713244-C-G

47501398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76713233-G-T

47501613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76713009-G-C

47501941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712683-G-A

47501992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712634-A-G

http://identifiers.org/hco/18/GRCh38#47502013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76712591-C-A

47502013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712591-C-T

47502021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712583-T-C

47502045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712567-G-A

47502046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712566-G-A

47502053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712559-G-T

47502060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712552-C-T

47502122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712489-A-G

http://identifiers.org/hco/18/GRCh38#47502141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76712470-C-A

47502141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712470-C-T

47502212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712397-G-A

47502338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712268-A-G

47502349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712257-A-G

47502353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712253-A-G

47502355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712251-G-A

47502355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712251-G-T

47502375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712231-T-A

47502375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712231-T-C

47502376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712230-A-G

http://identifiers.org/hco/18/GRCh38#47502390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76712216-C-A

47502411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712195-G-T

47502485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712134-G-T

http://identifiers.org/hco/18/GRCh38#47502573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76712074-C-A

47502573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712074-C-G

47502596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712052-A-G

47502604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76712044-G-A

47502650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76711991-G-A

47502650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76711991-G-C

47502650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76711991-G-T

47502689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76711952-G-A

47502689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76711952-G-T

47502802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76711841-G-T

47502906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76711744-T-C

http://identifiers.org/hco/18/GRCh38#47502911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76711739-C-A

47502911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76711739-C-T

http://identifiers.org/hco/18/GRCh38#47502962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76711685-C-A

47502978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76711659-G-T

47503097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76711208-G-A

47503229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76711081-C-G

47505024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76708961-T-A

47505106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76708888-C-T

47505112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76708882-G-A

47505186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76706721-G-A

47505338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76706568-T-C

http://identifiers.org/hco/18/GRCh38#47505351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76706555-A-C

47505441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76706492-T-C

47505506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76706425-G-T

47505708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76706235-C-T

http://identifiers.org/hco/18/GRCh38#47505713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76706230-C-A

47505713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76706230-C-T

http://identifiers.org/hco/18/GRCh38#47506068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76705569-A-C

47506107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76705528-T-G

47506654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76704367-G-T

47506809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76704149-T-A

47507521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76703485-A-G

47507781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76703235-A-G

http://identifiers.org/hco/18/GRCh38#47507790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76703226-C-A

47507799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76703217-C-T

47507835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76703178-G-A

47508704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76702153-T-C

47508879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76701974-A-G

47508879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76701974-A-T

47509145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76701727-C-T

47509202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76701663-G-A

47509505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76701461-T-C

47510049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76700960-G-A

47510059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76700950-A-T

http://identifiers.org/hco/18/GRCh38#47510081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76700928-A-C

47510227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76700790-C-G

47511150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76700258-G-A

47511546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76699849-C-T

47511784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76699626-C-T

47511989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76699387-T-A

47511989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76699387-T-C

http://identifiers.org/hco/18/GRCh38#47511995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76699381-C-A

47512738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76698619-C-T

47513185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76698160-C-T

47513224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76698122-C-T

47513609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76697735-G-A

47513615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76697729-G-T

47513616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76697728-A-T

47514736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76697041-G-A

47516145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76694092-C-T

http://identifiers.org/hco/18/GRCh38#47518982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76692344-C-A

47519031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692297-G-A

http://identifiers.org/hco/18/GRCh38#47519206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76692143-A-C

47519264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692084-A-T

47519310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692047-G-C

47519428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691976-T-C

47520165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691181-T-C

47520214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691149-G-A

47520266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691116-G-C

http://identifiers.org/hco/18/GRCh38#47520379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76691048-C-A

47520379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691048-C-G

47520379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691048-C-T

47520384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691043-G-A

47520384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691043-G-C

47520384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691043-G-T

47520753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76690695-C-G

47520753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76690695-C-T

http://identifiers.org/hco/18/GRCh38#47521745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76689240-C-A

47521745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76689240-C-T

47521752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76689233-T-A

47521902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76689124-T-C

47521926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76689096-C-G

47524546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76684672-T-C

47524658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76684590-C-T

47524708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76684554-T-A

47524769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76684496-G-T

47524878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76684392-G-T

47524952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76684314-T-C

47525049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76684218-G-A

47525275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683986-A-G

47525304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683957-G-A

47525336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683938-T-A

47525596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683722-A-G

47525811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683506-T-G

47526120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683214-C-T

47526132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683202-T-C

47526137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683197-G-T

47526348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682998-C-T

47526365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682979-C-T

47526377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682969-C-T

47526464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682898-G-T

47526842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682287-G-T

47528578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682240-C-T

47528820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682017-C-T

47528842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76681997-T-A

47528862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76681979-A-G

47528863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76681978-C-T

47528917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76681925-G-A

47529042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76681773-A-G

47529048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76681767-G-A

47529050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76681765-T-C

47529267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76681311-G-A

47529345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76681248-G-A

47529376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76681217-T-C

http://identifiers.org/hco/18/GRCh38#47529569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76680167-C-A

47529569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76680167-C-T

47529586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76680150-T-C

47529980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76679817-C-T

47530215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76679514-T-G

47530284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76679447-G-A

47530284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76679447-G-T

47530609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76679145-A-G

47530770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76679016-T-C

47530808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76678978-C-T

47530932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76678856-T-C

47531096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76678624-T-G

47531154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76678587-G-A

47531154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76678587-G-T

47531365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76678408-A-G

47531523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76678338-C-T

47531641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76678236-A-T

47531861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76678025-T-A

47531861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76678025-T-G

47531927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677987-C-T

47532014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677952-G-A

47532024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677943-G-A

47532217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677759-A-G

47532245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677731-A-G

47532246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677730-T-C

47532246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677730-T-G

47532266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677710-C-T

47532267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677709-A-G

47532387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677604-C-T

47533264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677301-G-A

47533288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677272-G-A

http://identifiers.org/hco/18/GRCh38#47533398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76677168-C-A

47533461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76677063-G-A

47533765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76676855-C-T

47533788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76676824-G-A

47533796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76676817-A-G

47533875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76676738-C-T

47533890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76676723-G-T

47533980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76676635-T-C

47538256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76665391-C-T

47538281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76665366-T-A

47538304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76665344-A-G

47538471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76665176-C-G

47538625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76665027-C-T

47538646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76665006-A-T

http://identifiers.org/hco/18/GRCh38#47538671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76664981-A-C

47538671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76664981-A-G

47538748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76664891-G-A

http://identifiers.org/hco/18/GRCh38#47542396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76662437-C-A

http://identifiers.org/hco/18/GRCh38#47542403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76662430-A-C

47542545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76662286-T-C

47542556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76662275-C-G

47543420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76661531-C-T

http://identifiers.org/hco/18/GRCh38#47543548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76661069-A-C

47543548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76661069-A-G

47543576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76661042-T-A

47543576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76661042-T-C

http://identifiers.org/hco/18/GRCh38#47543743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76660910-A-C

47543817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76660835-G-A

47543817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76660835-G-T

47543914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76660739-G-C

47545549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76660128-T-C

47545555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76660122-C-T

47545586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76660091-C-T

47545659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76660019-T-C

http://identifiers.org/hco/18/GRCh38#47545664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76660014-C-A

47545664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76660014-C-T

47545773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659913-G-T

http://identifiers.org/hco/18/GRCh38#47545778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76659908-A-C

47545778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659908-A-G

http://identifiers.org/hco/18/GRCh38#47545810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76659884-C-A

47545810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659884-C-T

47545867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76659806-G-A

47546153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659508-C-G

47546197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659465-G-C

47546332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659360-T-C

47546341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659357-T-G

47546342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659356-C-G

47546342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659356-C-T

47546477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659255-C-G

47546477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659255-C-T

47546577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659127-T-C

47546601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659104-A-T

47546619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76659086-G-A

47546728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76658994-C-G

47546728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76658994-C-T

47546759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76658963-G-T

47546785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76658942-T-C

47546935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76658842-A-G

47547088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76658697-C-T

47547089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76658696-G-A

47547649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76658334-G-C

47547680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76658313-G-T

47547767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76658231-G-A

47548041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76658055-C-T

47548096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76657995-A-G

47548252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76657806-T-G

47548262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76657796-T-C

47548274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76657768-T-G

47548330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76657728-T-C

47548366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76657695-C-T

http://identifiers.org/hco/18/GRCh38#47548506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76657542-C-A

47549186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76656927-C-T

47549294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76656845-A-G

47550020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76655263-C-T

47550091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76655190-G-C

47550135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76655166-C-T

47550461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76654924-G-C

47550890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76654554-C-T

47550943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76654502-C-T

http://identifiers.org/hco/18/GRCh38#47551075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76654395-A-C

47551266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76654241-A-T

47551502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76654100-C-T

47551540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76654067-C-T

47551577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76654031-A-G

http://identifiers.org/hco/18/GRCh38#47551701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76653916-C-A

47551702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76653915-C-T

47553015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76652879-A-G

47553254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76652652-A-G

47553922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76652020-A-G

http://identifiers.org/hco/18/GRCh38#47553943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76652001-C-A

47553943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76652001-C-T

47554730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76651759-T-C

http://identifiers.org/hco/18/GRCh38#47554779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76651726-A-C

47554779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76651726-A-G

47554782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76651723-C-T

47555247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76651332-A-G

47555823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76650811-A-G

47555866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76650771-C-G

47555884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76650749-C-T

47555914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76650721-C-T

47556250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76650087-G-C

47556256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76650081-T-C

47556570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76649789-G-A

47557251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76648271-C-T

47557350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76648195-C-T

47557386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76648177-T-C

47557470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76648091-T-A

47557470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76648091-T-C

47557547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76648015-T-C

47557548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76648014-G-T

47557553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76648009-T-G

http://identifiers.org/hco/18/GRCh38#47557637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76647901-A-C

47557644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647896-A-G

47557731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647820-G-A

47557853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647723-C-T

47557923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647654-C-T

47557947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647630-A-T

47558077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647525-G-A

47558298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647307-A-G

47558304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647301-G-T

47558313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647293-T-C

47558429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647181-T-C

http://identifiers.org/hco/18/GRCh38#47558433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76647177-C-A

47558433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647177-C-T

47558434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647176-G-A

47558464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76647146-G-T

http://identifiers.org/hco/18/GRCh38#47558478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76647124-C-A

http://identifiers.org/hco/18/GRCh38#47558695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76646899-C-A

47558712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76646885-C-G

47559217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645991-G-A

47559251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645957-G-A

47559333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645937-T-C

47559333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645937-T-G

47559568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645749-C-T

47559802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645614-G-C

47559987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645464-G-A

47560107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645373-T-G

47560167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645315-G-A

47560252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645230-G-A

47560252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645230-G-C

47560331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645154-G-C

47560459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76645021-G-A

47560544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76644956-C-T

47560728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76644798-T-C

http://identifiers.org/hco/18/GRCh38#47560773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76644755-C-A

47560810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76644728-C-T

47560907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76644609-C-T

47560999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76644523-A-G

47560999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76644523-A-T

http://identifiers.org/hco/18/GRCh38#47561058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76644465-C-A

http://identifiers.org/hco/18/GRCh38#47561574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76643952-A-C

47561761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76643737-G-C

47561761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76643737-G-T

47561777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76643714-T-C

47561819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76643677-A-G

http://identifiers.org/hco/18/GRCh38#47561957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76642835-C-A

47562124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76642663-T-G

47565310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76642514-G-A

http://identifiers.org/hco/18/GRCh38#47565321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76642502-C-A

47565348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76642475-G-T

47565432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76642423-T-G

http://identifiers.org/hco/18/GRCh38#47565483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76642369-A-C

47565795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76642080-G-C

47565799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76642076-A-T

47565815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76642060-G-A

47565833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76642042-T-C

47566171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76641715-C-G

47566307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76641590-C-G

47566307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76641590-C-T

47567847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76641120-T-A

47567847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76641120-T-C

47568045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76640915-G-T

47568236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76640718-G-A

47568282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76640673-G-A

47568362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76640608-G-A

47568362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76640608-G-C

47568440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76640528-A-G

47568497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76640471-A-T

http://identifiers.org/hco/18/GRCh38#47568613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76640368-A-C

47569785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76639990-A-G

47569886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76639900-C-T

47569960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76639818-C-T

47569999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76639781-T-G

47570028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76639755-T-C

47570095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76639698-A-G

47570405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76639479-G-A

47570670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76639289-G-T

47570937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76639166-C-T

47570995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76639119-G-A

47571448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76638819-A-G

http://identifiers.org/hco/18/GRCh38#47572522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76637572-C-A

47572573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76637527-C-T

47572679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76637440-T-C

47573267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636925-G-A

47573307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636895-T-C

47573471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636731-G-C

47573503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636698-C-G

47573521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636676-T-A

http://identifiers.org/hco/18/GRCh38#47573547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76636651-C-A

47573547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636651-C-T

47573558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636642-G-A

47573558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636642-G-C

http://identifiers.org/hco/18/GRCh38#47573646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76636552-C-A

47573646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636552-C-T

47573648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636550-T-A

47573750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636463-G-A

47573801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636418-G-C

47573851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636379-T-A

47574226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636120-G-A

47574325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76636018-C-T

47574483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76635849-G-T

47574496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76635836-T-C

http://identifiers.org/hco/18/GRCh38#47574580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76635755-C-A

47574580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76635755-C-T

47574625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: non coding transcript exon variant
orthologous variants: 76635712-G-T

47574707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: non coding transcript exon variant
orthologous variants: 76635635-C-T

47574798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76635546-G-A

47574798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76635546-G-T

47575005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76635337-A-G

47575005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76635337-A-T

47575087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76635261-G-A

47575194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76635198-C-T

47575323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76635062-C-G

47575421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76634967-A-G

47575476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76634910-A-G

47575530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76634865-G-A

47575530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76634865-G-C

47576419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76634407-T-G

47576826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76634020-C-T

47576891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76633979-C-T

47577298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76633618-C-T

47577469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76633453-G-A

47577698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76633260-C-T

47579845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76632594-A-G

47580469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76632330-G-C

47581329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76631498-G-T

47581857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76631053-C-G

http://identifiers.org/hco/18/GRCh38#47581887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76631023-A-C

47581887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76631023-A-G

47581887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76631023-A-T

47582142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630792-A-T

47582163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630771-C-T

47582176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630749-C-T

47582207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630719-G-T

47582248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630679-T-A

47582504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630430-G-T

http://identifiers.org/hco/18/GRCh38#47582607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76630358-C-A

47582612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630356-T-C

47582804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630168-T-G

47582811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630140-G-A

47582811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630140-G-C

47582811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630140-G-T

47582815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630136-G-T

47582828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630123-G-T

http://identifiers.org/hco/18/GRCh38#47582869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76630082-C-A

47582869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630082-C-G

47582979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76630027-A-G

47583025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76629983-G-A

http://identifiers.org/hco/18/GRCh38#47583349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76629662-C-A

47583698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76629320-G-A

47583834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76629179-C-T

47584288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76628771-G-A

47584288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76628771-G-C

47584352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76628709-G-C

47584768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76627889-T-C

47584769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76627888-T-G

47585140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76627548-C-T

47585157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76627531-C-T

47585334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76627356-C-T

47585523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76627143-C-T

47585528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76627138-T-C

47585536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76627130-G-A

47585767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76626820-G-A

47587064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76626152-A-G

47587064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76626152-A-T

47587113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76626103-T-C

47587321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76625927-G-A

47587321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76625927-G-T

47587457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76625797-G-T

47587469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76625790-T-G

47587588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625692-T-C

47587831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76625417-G-A

47587847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76625401-G-C

http://identifiers.org/hco/18/GRCh38#47587884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76625375-A-C

47587884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76625375-A-G

47587922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76625350-T-C

http://identifiers.org/hco/18/GRCh38#47588569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76624700-C-A

47588867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76624410-G-A

47590401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76623937-G-A

47592438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76623698-T-C

47592591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76623539-C-T

47592658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76623479-G-A

47592703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76623436-T-C

47592800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76623306-A-G

47592842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76623264-G-A

47592843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76623263-G-T

47592989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76623114-G-A

47593510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622645-C-G

47593510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622645-C-T

47593540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622615-T-G

http://identifiers.org/hco/18/GRCh38#47593607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76622554-C-A

47593616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622545-C-T

47593636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622515-C-T

47593816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622325-A-G

47594229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: non coding transcript exon variant
orthologous variants: 76621960-G-A

47594229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: non coding transcript exon variant
orthologous variants: 76621960-G-T

47594268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: non coding transcript exon variant
orthologous variants: 76621921-A-G

47594268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: non coding transcript exon variant
orthologous variants: 76621921-A-T

http://identifiers.org/hco/18/GRCh38#47594490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#76621689-C-A

47594490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31724
most severe consequence: non coding transcript exon variant
orthologous variants: 76621689-C-T