214411094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70764907-G-T

http://identifiers.org/hco/2/GRCh38#214411330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#70765143-A-C

214411489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70765302-G-T

214411667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70765480-G-A

214411667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70765480-G-T

214412137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70765901-T-A

214412374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70766138-T-A

http://identifiers.org/hco/2/GRCh38#214412710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70766496-A-C

214412862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70766655-G-T

214413239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70767048-T-C

http://identifiers.org/hco/2/GRCh38#214413415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70767222-C-A

214413666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70767407-T-C

214414081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70767827-G-A

214414400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 70768144-T-C

http://identifiers.org/hco/2/GRCh38#214414463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#70768207-C-A

214414463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 70768207-C-T

http://identifiers.org/hco/2/GRCh38#214414783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70768473-C-A

214414783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70768473-C-T

214415183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70768840-G-C

214415183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70768840-G-T

214415232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70768872-G-T

214415346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70768984-G-T

214416030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70769658-G-A

214416055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70769684-G-C

214416088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70769731-C-T

214416120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70769754-C-T

214416169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70769801-A-G

214416315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70770172-G-C

214416335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70770192-T-A

214416465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70770299-A-G

214416567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70770387-A-G

214416621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70770442-G-C

214416788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70770589-T-C

214417102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70770887-T-C

214417184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70770967-T-C

214417519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70771456-A-T

214418261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70772216-T-A

214418423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70772315-G-A

214418553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70772425-T-C

214418911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70772815-T-C

214418977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70772852-A-G

214419067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70772937-G-A

214419212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70773074-A-G

214419252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70773116-G-C

214419278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70773137-A-G

http://identifiers.org/hco/2/GRCh38#214419363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70773236-A-C

214419420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70773289-T-C

214419546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70773413-C-G

214419660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70773529-G-A

214419662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70773531-G-C

214419839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70773718-A-T

214420455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70774105-G-A

http://identifiers.org/hco/2/GRCh38#214420527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70774169-A-C

http://identifiers.org/hco/2/GRCh38#214420584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70774229-C-A

214420722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70774375-A-G

214420722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70774375-A-T

http://identifiers.org/hco/2/GRCh38#214420807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70774449-C-A

214420870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70774512-T-G

214420925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70774563-A-G

http://identifiers.org/hco/2/GRCh38#214421234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70774855-A-C

214421236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70774857-T-C

214422280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70775521-G-C

214422384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70775633-T-G

214422428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70775686-G-C

214422508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70775786-T-C

214422566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70775847-T-C

214422823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70776103-A-G

214422847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70776127-C-G

214422921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70776202-A-G

214423496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70777251-C-T

214424376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70778259-G-C

214424516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70778395-A-G

http://identifiers.org/hco/2/GRCh38#214424636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70778506-A-C

214424992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70779696-C-T

214425315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70779954-G-A

214425363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70780000-T-C

214425607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70780238-A-G

214426629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70780854-G-A

214426803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70781043-A-G

214427024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70781391-G-C

214427146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70781753-C-T

214427151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70781798-T-A

214427191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70781841-C-T

214427479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70782135-G-T

214427539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70782190-T-A

214427539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70782190-T-G

214428061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70782580-A-G

214428061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70782580-A-T

http://identifiers.org/hco/2/GRCh38#214428076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70782595-C-A

http://identifiers.org/hco/2/GRCh38#214428172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70782747-A-C

214428367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70782993-A-G

http://identifiers.org/hco/2/GRCh38#214428381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70783007-A-C

214428391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783017-A-G

214428435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783069-T-C

214428580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783181-T-A

214428751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783363-T-A

214428839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783442-T-A

214428839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783442-T-C

214428839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783442-T-G

214429128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783703-T-G

214429155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783729-A-G

214429278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783853-A-G

214429324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783898-T-A

214429559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784105-C-T

214429586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784131-T-C

214429634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784172-T-C

214429785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784315-A-G

214430344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784676-T-C

214430496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785021-C-T

214430569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785104-T-C

214430569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785104-T-G

214430678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785207-T-C

214430706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785234-C-G

214430706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785234-C-T

214430963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785694-G-A

214430976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785707-T-A

214431346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786076-T-C

214431377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786110-T-A

214431426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786157-G-A

214431426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786157-G-T

214431527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786253-C-T

214431587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786312-A-T

214431721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786469-A-G

214431724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786472-C-G

214431766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786516-C-T

214431868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786612-G-A

214432054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786799-A-G

214432085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786830-A-T

http://identifiers.org/hco/2/GRCh38#214432117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70786862-A-C

214432117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786862-A-T

214432193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70786932-G-A

214433540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70788334-T-A

214435443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70788961-A-G

214435576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789119-T-C

214435661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789202-C-T

214436068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789572-G-A

214436093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789597-G-T

214436115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789619-T-A

214436115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789619-T-C

214436159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789658-G-A

214436169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789668-A-G

http://identifiers.org/hco/2/GRCh38#214436185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70789684-C-A

214436185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 70789684-C-T

214436232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70789728-A-T

214436256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70789751-A-G

214436260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70789755-T-C

214436295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70789789-G-A

214436295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70789789-G-C

214436305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70789799-G-C

214436359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789852-A-G

214436423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789899-C-T

214436444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789921-T-C

214436462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789939-G-A

214436462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789939-G-T

214436485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789962-G-A

214436485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70789962-G-T

214436542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70790009-G-A

214436825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70790292-T-A

http://identifiers.org/hco/2/GRCh38#214436832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70790299-C-A

214436877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70790344-G-A

214436877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70790344-G-T

http://identifiers.org/hco/2/GRCh38#214436902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70790372-C-A

214436903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70790373-A-G

214436913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70790383-G-A

214437008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70790478-T-C

214437270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70790754-C-T

214437335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70790818-G-C

214437590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70791074-G-A

214437590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70791074-G-C

214437851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70791314-G-T

http://identifiers.org/hco/2/GRCh38#214438233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70791690-A-C

214438321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70791778-G-A

214438414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70791858-G-T

214438523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70791953-T-G

214438541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70791971-C-T

http://identifiers.org/hco/2/GRCh38#214438827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70792248-A-C

http://identifiers.org/hco/2/GRCh38#214438831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70792252-A-C

214438870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70792298-G-A

214438870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70792298-G-C

214438944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70792369-C-G

214439027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70792463-T-C

214439038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70792472-G-T

http://identifiers.org/hco/2/GRCh38#214439091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70792525-C-A

214439295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70792712-A-G

214439295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70792712-A-T

214439487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70792889-T-C

214439962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70793309-T-A

214440323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70793689-A-G

214440577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70794296-A-G

http://identifiers.org/hco/2/GRCh38#214440714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70794393-A-C

214440746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70794425-A-G

214440772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70794450-C-T

http://identifiers.org/hco/2/GRCh38#214440882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70794558-A-C

214440917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70794569-T-C

214440998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70794647-C-T

214441008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70794657-T-C

214441008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70794657-T-G

214441043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70794698-T-C

214441060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70794715-C-T

http://identifiers.org/hco/2/GRCh38#214441098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70794753-C-A

214441327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70794962-C-T

214441343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70794971-G-A

214441404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70795026-A-T

214441598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70795189-T-A

http://identifiers.org/hco/2/GRCh38#214441835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70795442-A-C

214442524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70796144-C-G

214442536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70796156-C-T

214442561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70796183-G-C

214442748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70796362-T-A

http://identifiers.org/hco/2/GRCh38#214443466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70796926-A-C

214445520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70800462-A-T

214445578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70800506-G-T

214445645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70800547-A-G

214445864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70800803-T-C

214446147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70801069-G-A

214446206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70801136-T-A

214446206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70801136-T-C

214448261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70801926-G-T

214448847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70802490-T-C

214448968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70802645-C-T

214449153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70802821-A-G

214449232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70802888-T-C

214449269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70802922-G-A

214449454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70803127-T-A

214449464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70803137-G-A

http://identifiers.org/hco/2/GRCh38#214449691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70803311-A-C

214449782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70803386-T-C

214449862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70803465-G-A

214449862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70803465-G-C

214449925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70803528-T-C

214449941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70803544-G-T

214450066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70803659-G-C

214450149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70803763-A-G

214450203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70803817-C-G

214450203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70803817-C-T

http://identifiers.org/hco/2/GRCh38#214450372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70803978-C-A

214450384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70803990-A-G

http://identifiers.org/hco/2/GRCh38#214450596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70804151-C-A

214450634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804189-G-A

214450642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804197-G-A

214450690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804229-T-C

214450690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804229-T-G

214450802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804341-A-G

214451055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804597-G-A

214451099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804641-G-A

214451302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804831-T-C

214451302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804831-T-G

214451324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804845-T-A

214451324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804845-T-C

214451324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804845-T-G

214451345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70804916-T-A

214451576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70805134-T-C

214451834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70805389-G-A

214451868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70805548-T-C

214451868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70805548-T-G

214452644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70806233-C-T

214452841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70806430-G-A

214453018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70806630-A-G

214453147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70806771-G-A

214453156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70806779-A-G

http://identifiers.org/hco/2/GRCh38#214453157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70806780-A-C

214453157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70806780-A-G

214453157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70806780-A-T

214453282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70806923-T-A

214466500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70808997-G-T

214466744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70809177-T-C

214466805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70809236-G-A

214466805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70809236-G-T

http://identifiers.org/hco/2/GRCh38#214466942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70809373-C-A

214467165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70809588-T-C

214467289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70809683-G-A

http://identifiers.org/hco/2/GRCh38#214467439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70809948-C-A

214467455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70809958-G-C

214467487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70809990-T-C

214467570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70810069-T-A

214467589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70810079-T-C

214467747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70810125-A-G

214467839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70810214-T-C

214468382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70810312-G-C

214468634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70810590-T-A

214468938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70810878-T-C

214469007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70810945-G-A

214469007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70810945-G-T

214469650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70811309-C-T

214470012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70811687-G-A

214470197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70811932-C-T

214470319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70812050-C-T

214471163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70814519-A-G

214471577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70814941-G-A

214471577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70814941-G-T

214471875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70815197-C-T

214472707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70815859-T-C

214473180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70816291-C-T

214473264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70816372-T-C

214473369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70816465-A-T

214473392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70816490-T-C

214473446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70816546-G-A

214473497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70816636-T-A

214473659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70816790-G-A

214473659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70816790-G-T

214473711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70816840-T-C

214473886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70817371-C-T

http://identifiers.org/hco/2/GRCh38#214473939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70817423-A-C

214474118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70817590-A-G

214474188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70817665-C-T

214474213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70817690-A-G

214474481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70818966-A-G

214474558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70819036-G-A

214474619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70819095-A-G

214474728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70819204-G-A

214474888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70819375-G-C

214475717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70820196-G-C

214475852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70820331-G-A

214475852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70820331-G-T

214475972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70820446-A-G

214475978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70820452-C-T

http://identifiers.org/hco/2/GRCh38#214476499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70820969-A-C

214476610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70821079-T-C

214476712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70821196-A-T

214476784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70821313-C-T

http://identifiers.org/hco/2/GRCh38#214477174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70821683-A-C

214477311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70821784-T-C

214477366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70821838-T-C

214477400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70821872-G-A

214477446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70821917-C-G

214477684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70822308-A-G

214477684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70822308-A-T

214477890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70822496-C-G

214477890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70822496-C-T

http://identifiers.org/hco/2/GRCh38#214478013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70822623-C-A

214478013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70822623-C-G

214478017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70822627-T-C

214478033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70822633-C-G

http://identifiers.org/hco/2/GRCh38#214478034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70822634-A-C

214479407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70824864-T-G

http://identifiers.org/hco/2/GRCh38#214479500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70824948-C-A

214480509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70825324-C-T

214480525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70825340-A-G

214480577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70825392-G-A

214480719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70825536-G-A

214480956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70825735-A-G

http://identifiers.org/hco/2/GRCh38#214481324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70826308-C-A

214481384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70826367-G-A

214481384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70826367-G-T

214481419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70826401-G-A

214481427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70826409-G-A

214482008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70827072-A-G

214482008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70827072-A-T

214482234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70827300-G-T

214482426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70827485-C-T

214482859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70827694-C-T

214482949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70827768-A-G

214483076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70827896-A-G

214483282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70828090-T-C

214483383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70828197-G-A

214483452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70828271-C-T

214483455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70828274-T-G

214483591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70828446-T-C

214483785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70828643-T-A

214483931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70828783-G-T

214484153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70828960-G-A

214484314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70829081-T-G

214484379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70829146-G-A

214484927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70830020-C-G

214485003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70830118-T-G

214485379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

214485429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

214485429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

214485454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

214485574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

214486352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70831500-G-A

214486723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70831829-A-G

214486913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70831954-T-A

214487029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70832067-G-T

214487074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70832115-A-T

214487185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70832223-T-C

214487319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70832337-T-G

214487547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70832547-C-T

214487622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70832618-A-G

214487641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70832637-G-C

214487729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70832735-G-A

214487906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70832916-A-G

214488016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70833024-A-G

214488100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70833096-C-T

214488157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70833151-G-A

214489428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70833646-G-A

214489477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70833693-A-G

214489479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70833695-G-A

http://identifiers.org/hco/2/GRCh38#214489556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70833760-C-A

214489703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70833889-T-C

214489801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834005-G-T

214489866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834069-C-T

214489910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834111-C-T

http://identifiers.org/hco/2/GRCh38#214489962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70834144-C-A

214490139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834193-G-C

214490139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834193-G-T

214490452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834504-G-C

214490512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834565-G-T

214490623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834688-G-T

214490625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834690-G-A

214490640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834705-C-G

214490640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834705-C-T

214490719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834762-A-G

214490996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70835040-G-C

http://identifiers.org/hco/2/GRCh38#214491474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70835579-A-C

214491533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70835635-A-G

214491755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70835835-G-A

214491755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70835835-G-T

214492377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70836456-G-A

214492533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70836617-G-C

214492603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70836669-T-C

214492644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70836706-A-G

214492820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70836865-T-A

214493832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70837676-G-A

214493889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70837727-T-A

214494058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70837920-T-A

214494065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70837927-G-A

http://identifiers.org/hco/2/GRCh38#214494082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70837949-C-A

http://identifiers.org/hco/2/GRCh38#214494372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70838249-C-A

214494372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70838249-C-T

214494450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70838309-C-G

214494648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70838509-G-A

214495371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839166-G-T

214495708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839572-T-C

214495777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839647-T-C

214495796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839667-G-A

214495844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839730-C-T

214495875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839773-A-G

214495889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839789-G-T

214495901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839802-G-A

214495901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839802-G-C

214495901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839802-G-T

214496328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70840359-A-G

214496709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70840745-C-T

214496984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842603-C-T

214497254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842875-T-G

214497284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842908-G-T

214498561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70843410-C-G

http://identifiers.org/hco/2/GRCh38#214498696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70843544-C-A

214498974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70843802-C-T

214499371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70843882-G-T

214499383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70843894-T-C

214499842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70844207-G-A

214499886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70844250-G-A

214500069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70844356-A-T

214500096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70844383-T-C

214500381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70844677-G-A

214500532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70844833-C-T

214500557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70844858-C-T

214500582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70844879-G-C

214500754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845049-T-C

214500886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845191-C-T

http://identifiers.org/hco/2/GRCh38#214501208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70845504-A-C

http://identifiers.org/hco/2/GRCh38#214501240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70845536-C-A

214501251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845547-C-T

214501865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845886-G-A

214501887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845908-C-T

214502027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70846041-T-G

214502733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70846416-G-T

214502853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70846503-C-T

214503089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70846719-G-A

214503292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70846909-G-A

214503292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70846909-G-C

214503409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848196-T-C

214503419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848208-T-C

214503459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848259-T-C

214503535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848335-A-G

214503539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848339-G-C

http://identifiers.org/hco/2/GRCh38#214503690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70848500-C-A

214503690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848500-C-T

214503707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848517-T-A

214503714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848524-G-A

214503730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848540-G-A

214503782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848568-T-G

214503787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848573-G-T

214503836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848619-G-A

214503911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848698-T-C

214503946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848733-A-G

214503979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848767-T-C

214504035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848822-T-A

214504095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848880-G-A

214504208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848998-G-A

214504376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849451-A-G

214504447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849524-T-A

214504454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849531-C-T

214504497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849574-C-G

214504510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849587-A-G

214504602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849678-G-A

214504721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849802-G-C

214504807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849886-A-G

http://identifiers.org/hco/2/GRCh38#214504914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70849980-C-A

214504952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70850018-C-G

http://identifiers.org/hco/2/GRCh38#214505007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70850071-A-C

214505040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70850104-T-G

214505230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70850303-G-A

214505301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70850374-C-T

214505328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70850401-A-G

214505445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70850501-G-C

214505486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70850566-T-A

214505775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70850863-A-G

214505851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70851027-A-G

214506565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70851713-C-T

214506698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70851777-G-A

214507086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852334-G-A

http://identifiers.org/hco/2/GRCh38#214507238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70852797-A-C

214507372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852926-G-C

214507657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853210-T-C

214507670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853223-T-C

214507927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853481-A-G

214507940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853496-T-A

214508218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853695-G-A

214508405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853778-G-T

214508794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854099-T-C

214508797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854102-T-C

214508822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854127-C-T

214509114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854332-G-A

214509114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854332-G-C

214509145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854354-T-C

214509339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854535-T-G

214509627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854757-C-G

214509702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854834-G-A

214509702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854834-G-T

http://identifiers.org/hco/2/GRCh38#214510111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70858401-C-A

http://identifiers.org/hco/2/GRCh38#214510174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70858470-C-A

214510221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858519-C-G

214510221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858519-C-T

214510378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858670-T-G

214510623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858909-T-C

214511340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70859426-T-C

214511525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70859570-T-G

214511607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70859633-T-G

214511625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70859646-G-A

214511625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70859646-G-T

214511823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70859786-A-T

214511844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70859806-T-C

214512008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70859904-T-C

http://identifiers.org/hco/2/GRCh38#214512042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70859941-C-A

214512772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70860392-G-A

214512942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70860562-C-T

214513390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70860971-A-G

214513409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70860990-T-C

214513666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70861271-T-C

214513740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70861356-G-A

http://identifiers.org/hco/2/GRCh38#214513745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70861361-A-C

214513940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70861520-A-G

214513987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70861573-A-T

http://identifiers.org/hco/2/GRCh38#214514097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70861685-C-A

214514219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70861805-C-T

214514536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862105-C-T

214514725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862302-G-C

214514730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862307-C-T

http://identifiers.org/hco/2/GRCh38#214514738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70862315-A-C

214514821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862411-G-A

214515154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862744-G-A

214515179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862769-T-G

214515395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862984-G-A

214515950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863186-C-G

214515950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863186-C-T

214516076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863298-T-C

214516177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863406-G-A

214516182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863411-A-G

214516249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863477-G-A

214516305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863530-C-G

214516327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863552-A-G

214516575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863791-T-C

214516760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863972-T-C

214516778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863991-T-C

214517231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865835-C-T

214517267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865868-A-G

214517310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865908-T-C

214517332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865930-G-T

214517503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866078-A-T

214517549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866117-G-C

214517610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866174-G-A

214517717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866266-T-C

214517718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866267-A-G

214517915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866460-C-T

214517916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866461-C-G

214518556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70867421-C-T

214518857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70867678-T-C

214519080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70867875-G-A

214519265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70868088-G-A

214519309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70868132-C-T

214519475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70868256-T-C

214519484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70868265-A-G

214519497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70868278-T-C

http://identifiers.org/hco/2/GRCh38#214519552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70868311-A-C

214520691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70868958-C-T

214520789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70869054-A-G

214521711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70869602-A-G

214521711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70869602-A-T

214521730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70869620-C-T

214522027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70869886-C-T

214522607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870002-A-T

214522759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870145-T-C

214523111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870549-G-C

http://identifiers.org/hco/2/GRCh38#214523182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70870625-A-C

214523379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870814-A-T

214524091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70871807-A-G

214524109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70871825-T-C

214524148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70871868-A-G

214524148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70871868-A-T

214524601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872570-G-A

214524627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872588-G-A

214524631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872592-C-G

214524635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872596-T-C

214524719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872660-A-T

214524866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872814-G-A

214524882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872837-C-T

214525211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70873390-G-T

214525296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70873483-G-T

214525326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70873501-G-A

http://identifiers.org/hco/2/GRCh38#214525332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70873507-C-A

214525336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70873516-C-T

214525606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70873789-G-A

214525658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70873834-C-T

http://identifiers.org/hco/2/GRCh38#214526546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70874355-A-C

214526547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70874356-G-A

214526646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70874451-C-G

http://identifiers.org/hco/2/GRCh38#214528042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70875078-A-C

http://identifiers.org/hco/2/GRCh38#214528191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70875361-A-C

214528639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70875810-T-C

214528715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70875893-A-G

214528809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70875976-C-T

214529160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70876319-A-G

214529308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70876454-G-A

214529553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70876855-A-G

214529608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70877055-G-A

214529956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70877399-C-T

214530544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70877996-C-T

214530915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70878355-G-A

214531183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70878675-G-A

214531253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70878869-T-C

214531284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879080-A-G

214531441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879238-T-C

214531660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879459-T-C

214531662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879461-C-T

214531714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879504-G-C

214532482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880212-T-C

214532482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880212-T-G

http://identifiers.org/hco/2/GRCh38#214532490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70880220-A-C

214532490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880220-A-T

214532542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880290-T-C

214533075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880803-G-A

214533676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70881446-C-G

214533695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70881465-T-G

214534174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70881934-C-T

214534204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70881963-T-A

214534204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70881963-T-C

214534311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882078-T-C

214534399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882169-C-T

214534408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882178-T-C

214534489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882247-T-G

214534605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882362-A-T

214535324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70883322-A-T

214535640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70883614-C-T

214535912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70884484-G-A

214535940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70884513-C-T

214536905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885558-T-C

214537000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885625-G-A

214537000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885625-G-C

214537000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885625-G-T

214537364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885976-G-A

214537530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70886128-G-C

214537540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70886136-G-A

214537540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70886136-G-T

214537656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70886529-T-A

214537862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70886729-T-C

214537938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70886775-G-T

214538166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887026-G-T

214538325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887139-C-T

214538422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887237-A-G

214539109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887873-G-A

214539583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70888331-A-G

214539992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70888761-A-T

http://identifiers.org/hco/2/GRCh38#214540018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70888788-C-A

214540018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70888788-C-T

214541281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70890035-A-G

214541917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70890773-T-A

http://identifiers.org/hco/2/GRCh38#214541998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70890859-C-A

214542556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891424-C-T

214542610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891479-C-T

214542697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891566-T-C

214542736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891605-C-T

214543254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70892267-A-T

http://identifiers.org/hco/2/GRCh38#214543364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#70892365-C-A

214543836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70892813-G-A

214543881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70892858-A-G

http://identifiers.org/hco/2/GRCh38#214543891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70892868-C-A

214543891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70892868-C-T

http://identifiers.org/hco/2/GRCh38#214544036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70893013-C-A

214544036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893013-C-T

214544093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893070-C-T

214544103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893080-A-T

214544156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893131-C-T

214544207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893187-T-C

214544360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893313-T-C

214544718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893631-A-G

214544786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893706-G-C

214544882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893797-T-C

214544882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893797-T-G

http://identifiers.org/hco/2/GRCh38#214544916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70893830-C-A

214544950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893864-T-G

214544960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893874-T-C

214546452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70895410-T-C

214546514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70895472-A-G

214547077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896041-A-T

214547078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896042-C-T

214547365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896261-T-C

214547814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896716-T-G

214547974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896860-G-C

214548005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896898-T-C

214548151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70897027-C-T

214548167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70897043-G-A

214548246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70897139-G-C

214548278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70897171-A-G

214550464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899019-T-A

214550771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899313-T-C

214550868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899429-C-T

http://identifiers.org/hco/2/GRCh38#214550930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70899491-C-A

214551026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899574-G-A

214551217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899749-T-C

214551267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899793-A-G

214551272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899798-G-T

214551577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900082-A-G

214551589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900094-G-A

214551589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900094-G-T

http://identifiers.org/hco/2/GRCh38#214551606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70900100-A-C

214551818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900303-T-C

214552063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900715-C-T

214555600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70901417-G-A

214555989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70901813-T-C

214556514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70902109-C-T

http://identifiers.org/hco/2/GRCh38#214557098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70902673-A-C

214557098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70902673-A-G

214559346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70903937-A-G

214559350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70903941-G-A

214559440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70904028-C-T

http://identifiers.org/hco/2/GRCh38#214559594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70904209-A-C

214559843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70904501-C-G

214560083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70904586-G-C

214560308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70904827-T-A

214560308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70904827-T-G

214560357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70904866-T-A

214560373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70904881-G-A

214560493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70904981-A-G

214560985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70905444-A-G

214561103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70905570-A-G

214561103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70905570-A-T

214561273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70905738-G-A

214561448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70905911-A-T

214561546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70905997-T-C

214561582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70906017-T-C

214561633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70906080-G-A

214561638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70906085-G-C

214564603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70906524-T-C

http://identifiers.org/hco/2/GRCh38#214564934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70906858-C-A

214565044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70906963-G-T

214565149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907067-G-T

214565239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907156-T-G

214565279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907183-T-G

214565477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907384-A-G

214565496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907402-A-T

214565514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907423-G-A

214565554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907472-T-A

214565876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907771-T-C

http://identifiers.org/hco/2/GRCh38#214565926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70907820-C-A

214565926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907820-C-T

214565944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907838-A-G

214565944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907838-A-T

214566095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907985-G-T

214566619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70908414-T-C

214566755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70908558-T-G

214566887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70908690-T-C

214567135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70908932-T-C

214567419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70909204-G-A

214567490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70909268-A-G

http://identifiers.org/hco/2/GRCh38#214567526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70909319-C-A

214567632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70909375-A-G

214567633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70909376-G-T

214567666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70909409-G-C

214567733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70909476-G-A

http://identifiers.org/hco/2/GRCh38#214567763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70909504-C-A

214568830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70910673-T-C

214569365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911197-T-C

214569487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911396-G-A

214569502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911411-C-T

214569540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911449-A-G

214569660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911541-T-A

214569748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911628-C-T

214569812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911688-A-G

214569941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911814-T-G

214570056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911947-C-T

214570354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70916751-A-T

214570663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70916763-G-T

214570703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70916799-T-C

214571346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70917485-T-C

http://identifiers.org/hco/2/GRCh38#214571402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70917539-A-C

214571405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70917542-G-A

214572948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70918517-C-T

214573098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70918660-C-T

214573113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70918675-T-C

214573192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70918748-G-T

214573360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70918934-G-C

214573381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70918955-A-G

214573431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70919005-A-G

214573716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70919273-T-C

214573728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70919283-C-T

214573729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70919284-T-C

http://identifiers.org/hco/2/GRCh38#214573761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70919316-A-C

214574255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70919508-C-G

214574255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70919508-C-T

http://identifiers.org/hco/2/GRCh38#214574293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70919547-A-C

214574695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70919946-T-C

214574780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70920031-G-T

http://identifiers.org/hco/2/GRCh38#214574791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70920070-A-C

http://identifiers.org/hco/2/GRCh38#214574835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70920146-C-A

214574844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70920155-C-G

214574844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70920155-C-T

214574904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70920222-T-C

214575037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70920367-A-T

214575170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70920584-C-T

214575787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 70921341-G-A

214575787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 70921341-G-C

214575831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70921385-C-G

214575842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70921396-G-A

http://identifiers.org/hco/2/GRCh38#214575861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70921414-C-A

214575861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70921414-C-T

http://identifiers.org/hco/2/GRCh38#214575982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70921539-A-C

http://identifiers.org/hco/2/GRCh38#214576133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70921697-C-A

214576133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70921697-C-T

214576431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70921976-T-C

214576432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70921977-G-A

214576432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70921977-G-T

214577104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70922650-A-G

214577187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70922720-G-C

214577187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70922720-G-T

214577253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70922797-G-T

http://identifiers.org/hco/2/GRCh38#214577262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70922805-C-A

http://identifiers.org/hco/2/GRCh38#214577270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70922813-C-A

http://identifiers.org/hco/2/GRCh38#214577280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70922823-C-A

214577282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70922825-A-G

214577298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70922841-T-A

214577354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70922885-G-A

214577439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70922976-T-C

214577747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70923268-T-A

214577747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70923268-T-C

214577890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70923411-T-A

214577920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70923441-G-T

214577941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70923462-A-G

214578233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70923774-G-A

http://identifiers.org/hco/2/GRCh38#214578253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70923788-A-C

http://identifiers.org/hco/2/GRCh38#214578273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70923808-C-A

214578314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70923849-G-C

http://identifiers.org/hco/2/GRCh38#214578481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70924040-C-A

214578481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70924040-C-T

214578482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70924041-T-C

http://identifiers.org/hco/2/GRCh38#214578527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70924084-C-A

214578527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70924084-C-T

http://identifiers.org/hco/2/GRCh38#214578634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#70924194-C-A

214578634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70924194-C-G

214578647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70924210-G-T

214578808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70924372-T-C

214578860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70924439-A-G