37590650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 64055857-G-A

37590650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 64055857-G-T

37590846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 64056053-T-C

37590873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 64056080-A-G

37590873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 64056080-A-T

http://identifiers.org/hco/4/GRCh38#37590946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64056153-C-A

http://identifiers.org/hco/4/GRCh38#37591016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64056223-C-A

37591016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64056223-C-T

37591030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64056237-G-A

37591030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64056237-G-T

37591081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64056269-G-A

37591081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64056269-G-T

http://identifiers.org/hco/4/GRCh38#37591130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64056325-C-A

37591130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64056325-C-T

http://identifiers.org/hco/4/GRCh38#37591292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64056476-A-C

http://identifiers.org/hco/4/GRCh38#37591353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64056540-C-A

http://identifiers.org/hco/4/GRCh38#37591524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64056690-C-A

http://identifiers.org/hco/4/GRCh38#37591677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64056829-C-A

37591741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64056890-A-G

http://identifiers.org/hco/4/GRCh38#37591746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64056895-C-A

37591746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64056895-C-T

37591756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64056907-G-T

37591770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64056921-A-G

37593565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64057169-C-T

37593628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64057232-T-C

37593638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64057242-G-A

37593927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64057538-G-A

37594057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64057717-T-A

37594057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64057717-T-C

37594094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64057754-G-C

37594142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64057791-C-G

37594218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64057870-T-A

37594379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058006-C-T

37594438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058059-T-A

37594443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058064-C-T

37594618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058463-C-G

37594716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058557-A-G

37595515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64060033-T-C

37595519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64060037-C-T

37595752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64060245-G-T

37596004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64060443-T-C

37596145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64060575-C-T

37596279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64060701-G-T

37596368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64060805-G-A

37596466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64060903-C-T

http://identifiers.org/hco/4/GRCh38#37596714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64061138-A-C

37596743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64061160-T-A

37596743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64061160-T-G

http://identifiers.org/hco/4/GRCh38#37600442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64062620-C-A

37600442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64062620-C-G

37600559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64062734-G-A

37600594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64062772-T-C

37602806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64063653-G-A

37602806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64063653-G-T

http://identifiers.org/hco/4/GRCh38#37602854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64063713-C-A

37602854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64063713-C-T

http://identifiers.org/hco/4/GRCh38#37602892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64063741-C-A

37602892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64063741-C-T

37602946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64063789-A-G

http://identifiers.org/hco/4/GRCh38#37603155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64063981-C-A

37603155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64063981-C-G

37610712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64066496-C-T

37610907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64066697-A-T

37610945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64066730-G-A

http://identifiers.org/hco/4/GRCh38#37611219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64067015-A-C

37611302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64067081-A-T

37611459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64067233-T-C

http://identifiers.org/hco/4/GRCh38#37612288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64067801-C-A

http://identifiers.org/hco/4/GRCh38#37612716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64067921-A-C

http://identifiers.org/hco/4/GRCh38#37612765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64067977-A-C

37612765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64067977-A-G

http://identifiers.org/hco/4/GRCh38#37612790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64068002-C-A

37612790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64068002-C-T

37613127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64068269-G-T

37613186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64068329-G-A

37613345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 64068497-G-A

37613428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64068578-A-G

37614450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070011-A-T

http://identifiers.org/hco/4/GRCh38#37614671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64070201-C-A

37614673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070203-T-A

37614692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070222-A-G

37614713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070231-G-A

37614756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070281-A-G

37614871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070372-A-G

37615022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070659-C-T

37615023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070660-C-T

37615264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070858-G-A

37615353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070938-C-T

http://identifiers.org/hco/4/GRCh38#37615363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64070947-C-A

37615546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64071864-T-G

37615698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64072000-C-T

37615745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64072025-A-T

37615829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64072107-T-C

37620361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64073333-C-G

37620366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64073338-G-T

37620431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64073409-C-G

37620454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64073420-A-G

37620459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64073425-C-T

37620963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64073913-G-C

37620968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64073920-T-A

37620968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64073920-T-C

37621432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64074347-G-A

37621432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64074347-G-C

37623476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64074938-G-T

37623502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64074961-G-A

37623627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075085-G-A

http://identifiers.org/hco/4/GRCh38#37623628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64075086-C-A

37623628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075086-C-T

37623642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075128-A-G

37623692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075174-T-C

37623774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075234-G-T

37623802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075249-C-T

37624941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64076138-C-G

37625024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64076220-G-A

37625024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64076220-G-T

37627283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64077588-G-A

37627936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64078787-G-A

http://identifiers.org/hco/4/GRCh38#37628061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64078884-C-A

http://identifiers.org/hco/4/GRCh38#37628082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64078904-A-C

37628212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64078985-C-T

37628330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64079092-T-C

37628511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64079164-T-C

37628945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64079579-G-A

37629007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64079695-A-G

37629170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64079942-G-C

37629311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64080167-T-C

http://identifiers.org/hco/4/GRCh38#37629503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64080362-C-A

37629660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64080672-C-T

37629786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64080792-C-G

37629859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64080865-A-G

37630037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64081043-G-T

37630118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64081113-T-C

37630241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64081190-G-A

37630241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64081190-G-T

37630318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64081261-T-G

37631033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64081813-G-A

37631266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64081984-G-T

37631309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082010-G-A

37631346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082039-C-T

http://identifiers.org/hco/4/GRCh38#37631358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64082051-C-A

37631358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082051-C-T

37631588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082287-G-A

http://identifiers.org/hco/4/GRCh38#37631601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64082300-A-C

37632871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082827-G-A

37633055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082942-T-C

37633447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082997-G-A

37633447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082997-G-T

37633453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64083003-T-G

37633597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64083141-G-A

37633597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64083141-G-T

37634053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64083553-G-A

http://identifiers.org/hco/4/GRCh38#37634361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64083839-C-A

37634455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64083920-C-T

37634567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084027-T-C

37634589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084049-T-A

37634759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084221-T-A

37634814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084259-A-G

37634840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084288-G-C

37634840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084288-G-T

http://identifiers.org/hco/4/GRCh38#37635142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64084587-C-A

37635142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084587-C-T

37635206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084662-G-T

http://identifiers.org/hco/4/GRCh38#37635241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64084672-C-A

37635241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084672-C-T

37635288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084718-C-G

37635343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084769-C-T

37635954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64085288-G-A

37636126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64085447-G-A

37636219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64085571-G-C

37636731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64085772-G-C

37636835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64085852-C-G

37636897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64085919-G-C

37636999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086017-T-C

37637023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086038-C-T

37637202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086180-G-A

http://identifiers.org/hco/4/GRCh38#37637355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64086341-C-A

http://identifiers.org/hco/4/GRCh38#37637511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64086466-C-A

37637543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086500-A-G

37637581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086527-C-G

37637598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086537-C-T

37637807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086729-T-C

37637820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086742-T-A

37637915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086840-T-G

37637930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086855-T-C

37637930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086855-T-G

37637948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086873-T-C

37637953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086878-C-T

37638184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087567-G-A

37638184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087567-G-C

37638208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087595-C-T

37638229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087609-G-A

37638294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087675-C-G

http://identifiers.org/hco/4/GRCh38#37638337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64087716-A-C

37638337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087716-A-G

37638394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087771-T-C

37638510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 64087884-G-A

37638510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 64087884-G-T

http://identifiers.org/hco/4/GRCh38#37638565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64087920-C-A

37638565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087920-C-T

37638589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087944-T-A

37638589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087944-T-C

37638592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087947-T-C

37639450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088085-C-T

37639504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088134-T-A

37639556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088187-C-T

37639590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088221-T-C

37639847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088468-A-G

37639997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088606-T-A

37640115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088754-C-T

37640117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088756-T-C

37640125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088764-T-C

http://identifiers.org/hco/4/GRCh38#37640192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64088829-C-A

37640214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088864-A-G

37640327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088988-T-C

37640458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64089113-G-A

37642648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64090237-G-T

http://identifiers.org/hco/4/GRCh38#37642748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64090319-C-A

37642748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64090319-C-T

37643352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64090846-A-G

37643568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64091189-C-T

37643589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64091210-C-T

37643694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64091288-T-C

37643779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64091373-T-C

37647250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64093262-T-A

37647250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64093262-T-G

37647437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 64093435-A-G

37647461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64093455-G-T

37647467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64093461-A-G

37647505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64093507-T-G

http://identifiers.org/hco/4/GRCh38#37647521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64093523-A-C

37647563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64093565-T-C

http://identifiers.org/hco/4/GRCh38#37647669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64093685-C-A

37647705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64093718-C-T

http://identifiers.org/hco/4/GRCh38#37647980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64093974-A-C

37647980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64093974-A-G

37647980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64093974-A-T

37648057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64094056-C-T

37648058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64094057-G-A

37648058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64094057-G-T

37648790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64094759-G-A

37649211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095078-T-C

37649224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095089-A-G

http://identifiers.org/hco/4/GRCh38#37649412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64095285-A-C

37649412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 64095285-A-G

http://identifiers.org/hco/4/GRCh38#37649470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64095346-C-A

37649470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64095346-C-G

37649470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64095346-C-T

http://identifiers.org/hco/4/GRCh38#37649485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64095361-C-A

37649485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64095361-C-G

37649485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64095361-C-T

37649511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095387-A-G

37649517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095393-G-T

37649573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095432-T-C

37649620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095485-A-T

37649816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095628-C-T

37650229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095912-G-A

37650384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64096062-T-C

37650430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64096097-A-G

37650774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64096357-C-T

37652100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64097642-T-C

37652130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64097672-C-T

http://identifiers.org/hco/4/GRCh38#37652196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64097726-A-C

37652196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64097726-A-G

http://identifiers.org/hco/4/GRCh38#37652297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64097826-C-A

37652501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64098429-T-C

37652637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64098537-A-T

37652671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64098569-G-C

http://identifiers.org/hco/4/GRCh38#37652787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64098677-C-A

37658470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64102861-A-T

37658568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64102953-G-A

37658669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64103049-C-T

37658809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64103179-G-A

37661915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64105839-C-T

37662126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64106024-C-T

http://identifiers.org/hco/4/GRCh38#37662398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64106270-C-A

37662401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64106273-G-A

37662436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64106308-A-G

37662440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64106312-C-T

http://identifiers.org/hco/4/GRCh38#37662456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64106327-A-C

37662463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64106333-G-C

37662507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64106379-A-T

http://identifiers.org/hco/4/GRCh38#37662530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64106400-C-A

37663115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64106932-G-A

37663203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64107025-C-T

37663220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64107042-A-G

37663281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64107105-G-A

37663323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64107147-G-C

37664489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64107895-T-C

37664806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64108239-G-A

37664969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64108357-T-C

37665112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64108509-G-T

http://identifiers.org/hco/4/GRCh38#37665127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64108524-C-A

37665257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 64108643-T-A

37665257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 64108643-T-C

37665257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 64108643-T-G

37665272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 64108658-T-A

37665275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 64108660-T-C

37665334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 64108684-C-T

37665365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64108714-G-T

37665452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64108792-G-T

37665461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64108801-A-T

http://identifiers.org/hco/4/GRCh38#37665478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64108817-C-A

37665478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64108817-C-T

37665499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64108839-G-A

37665499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64108839-G-T

37665577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64108916-T-C

http://identifiers.org/hco/4/GRCh38#37665674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64109008-C-A

http://identifiers.org/hco/4/GRCh38#37665697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#64109035-C-A

37665783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64109108-C-G

37665817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64109149-G-A

37665980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64109298-C-T

37666034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64109340-G-A

http://identifiers.org/hco/4/GRCh38#37666739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#64111015-C-A

37666739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64111015-C-T

37667100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64111389-C-T

37667159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64111432-T-C

37667159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64111432-T-G

37670023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64111998-A-G

37670108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112088-C-T

http://identifiers.org/hco/4/GRCh38#37670137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64112120-C-A

37670172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112155-T-C

37670226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112220-G-A

37670226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112220-G-T

37670236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112232-G-T

37670282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112275-G-A

37670322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112354-G-A

37670330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112362-A-G

37670438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112465-T-C

37671938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64113093-C-G

37672000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64113129-G-A

37672158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64113270-A-T

37672463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64113518-T-C

37672463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64113518-T-G

37672684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64113659-T-C

37672889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64113858-G-A

37672912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64113880-G-A

37673515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64114057-T-C

37673680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64114253-C-T

37673783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64114354-T-C

37673863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64114452-T-G

37673960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64114537-A-G

37673967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64114544-T-A

37674227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64114780-A-G

37674705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64115227-A-G

37675272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64116395-G-A

37675287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64116403-G-A

37675321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64116437-T-C

37675526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64116617-T-C

37675730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64116809-T-C

37675751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64116828-A-T

37676423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64118310-C-T

37676544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64118413-C-T

37676912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64118882-C-T

37676919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64118889-G-A

37677005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64118954-C-T

37677031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64118981-T-C

http://identifiers.org/hco/4/GRCh38#37677194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64119127-A-C

37677196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64119129-G-A

37677207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64119140-G-T

37677249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64119185-G-A

37677427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64119367-G-A

37678461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64119636-G-A

37678484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64119663-A-G

37678551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64119758-C-T

37678655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64119874-G-A

http://identifiers.org/hco/4/GRCh38#37678764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64119990-A-C

http://identifiers.org/hco/4/GRCh38#37681941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64122246-A-C

37681986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64122288-T-G

http://identifiers.org/hco/4/GRCh38#37682025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64122328-A-C

37682025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64122328-A-G

37682371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64123032-T-C

37682371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64123032-T-G

37682991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64123676-G-A

37682991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64123676-G-T

37683051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64123841-T-G

37683167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64124003-A-T

37683214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64124050-T-C

http://identifiers.org/hco/4/GRCh38#37683357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#64124178-A-C

37684182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64124335-C-G

37684233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64124359-A-G

37684306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64124431-T-G

37685041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64124847-C-T

37685433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64125250-A-T

37685438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64125255-G-A

37685796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64125602-G-T

http://identifiers.org/hco/4/GRCh38#37685814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64125620-C-A

37685814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64125620-C-G

37685998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64125773-C-T

http://identifiers.org/hco/4/GRCh38#37686057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#64125831-A-C

37686057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64125831-A-T

http://identifiers.org/hco/4/GRCh38#37686144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#64125938-C-A

37686144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64125938-C-T

http://identifiers.org/hco/4/GRCh38#37686148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#64125942-C-A

37686148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64125942-C-T

37686172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64125960-G-A

37686172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64125960-G-T

37686184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64125972-A-G

http://identifiers.org/hco/4/GRCh38#37686308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#64126097-C-A

37686308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27379
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 64126097-C-T