70299010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61418530-T-C

70299012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61418528-G-A

70299012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61418528-G-T

70299039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61418500-T-C

70299080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61418461-G-A

70299080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61418461-G-T

http://identifiers.org/hco/10/GRCh38#70299254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61418338-C-A

70299254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61418338-C-G

70299316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61418277-G-T

70299322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61418271-G-T

70299345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61418249-A-G

http://identifiers.org/hco/10/GRCh38#70299396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61418212-C-A

70299425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61418174-T-C

70299447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61418151-T-C

70299517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417595-T-C

70299643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417519-G-C

70299666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417494-A-G

70299668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417492-G-T

http://identifiers.org/hco/10/GRCh38#70299698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61417461-C-A

70299698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417461-C-T

70299699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417460-T-C

70299700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417459-T-A

70299700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417459-T-C

70299820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417388-A-G

http://identifiers.org/hco/10/GRCh38#70299892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61417324-C-A

70299911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417305-A-G

70299978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417242-G-A

70300043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417213-C-T

70300086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417180-G-A

70300086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417180-G-T

70300111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417155-G-T

70300129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417137-G-A

70300129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417137-G-T

http://identifiers.org/hco/10/GRCh38#70300145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61417121-C-A

70300145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417121-C-T

70300289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61417014-T-G

70300546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416824-C-T

70300615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416726-A-G

70300706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416663-G-C

70300706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416663-G-T

70300711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416658-C-T

70300725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416644-A-G

70300725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416644-A-T

70300732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416637-T-C

70300739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416630-G-A

70300739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416630-G-T

70300858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416546-G-A

70300858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416546-G-T

http://identifiers.org/hco/10/GRCh38#70300868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61416536-A-C

70300868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416536-A-G

70300882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416522-G-A

70300882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416522-G-T

70300973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416440-T-C

http://identifiers.org/hco/10/GRCh38#70301028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61416395-A-C

70301028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416395-A-G

70301133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416279-G-A

http://identifiers.org/hco/10/GRCh38#70301173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61416241-C-A

70301173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416241-C-T

http://identifiers.org/hco/10/GRCh38#70301184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61416230-C-A

70301239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416174-T-G

http://identifiers.org/hco/10/GRCh38#70301266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61416148-A-C

70301266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416148-A-G

70301338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416077-G-A

70301346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416069-A-G

70301350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61416065-T-G

70301359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61416056-G-A

70301359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61416056-G-T

70301409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61416006-A-G

70301522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61415893-A-G

70301574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61415849-G-A

70301574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61415849-G-T

70301575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61415848-G-A

70301575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61415848-G-T

70301580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61415840-G-A

70301580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61415840-G-C

70301580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61415840-G-T

70301647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61415788-G-A

70301647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61415788-G-C

70301647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61415788-G-T

http://identifiers.org/hco/10/GRCh38#70301653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61415782-C-A

70301653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61415782-C-T

70303537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61413469-G-A

70309414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61405406-C-G

70309417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61405403-T-C

70309481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61405356-C-G

70309741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61405137-G-A

70309742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61405136-T-G

http://identifiers.org/hco/10/GRCh38#70309815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61405066-C-A

70309879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61405029-C-T

70309981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404947-T-C

70310054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404907-T-A

70310054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404907-T-G

70311654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61403795-G-A

70311654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61403795-G-T

70311708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61403405-G-A

70311843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61403295-G-A

70311892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61403248-G-A

70311927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61403214-G-A

http://identifiers.org/hco/10/GRCh38#70311930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61403211-C-A

70312500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61402490-G-A

70312542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61402462-G-A

http://identifiers.org/hco/10/GRCh38#70313037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61400365-C-A

70313071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61400330-C-G

70313071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61400330-C-T

70313114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61400288-T-C

70313226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61400190-C-T

70316057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61398403-G-A

70316257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61398289-C-T

http://identifiers.org/hco/10/GRCh38#70316431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61398162-C-A

70316482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61398111-G-A

70316505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61398088-C-T

70316545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61398048-T-C

70316918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61397210-T-C

70317093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61397055-G-C

70317108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61397046-G-A

http://identifiers.org/hco/10/GRCh38#70319055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61391411-C-A

70319095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61391383-C-G

70319157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61391331-G-A

70319481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61391002-C-T

70319561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61390893-A-G

70319570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61390884-C-T

70319968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61389264-G-A

70319968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61389264-G-C

http://identifiers.org/hco/10/GRCh38#70320003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61389228-C-A

70320034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61389204-G-A

70320192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61389052-G-T

http://identifiers.org/hco/10/GRCh38#70320503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61388436-C-A

70320527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61388413-T-C

70320588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61388352-T-C

70320691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61388236-G-A

70320732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61388204-A-G

70320935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61387985-C-G

70320946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61387974-C-T

70320950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61387970-G-A

70321013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61387918-C-T

70321316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61386548-C-T

70321773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61386129-A-T

70322365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61385609-T-A

70322392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61385544-G-A

70322394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61385542-G-C

http://identifiers.org/hco/10/GRCh38#70322479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61385453-A-C

70322524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61385366-C-T

70322525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61385365-T-C

70322809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384955-A-G

http://identifiers.org/hco/10/GRCh38#70322885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61384723-C-A

70322986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384632-T-C

70322989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384629-C-T

70323136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384502-G-A

70323150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384488-C-T

70323227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384416-C-G

70323227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384416-C-T

70323446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384280-C-T

70323692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384181-G-C

http://identifiers.org/hco/10/GRCh38#70323742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61384134-C-A

70323742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384134-C-T

70323767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384108-G-A

70323767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384108-G-C

70323767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384108-G-T

70323773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384102-C-T

70323799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384042-G-A

70323799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384042-G-T

http://identifiers.org/hco/10/GRCh38#70323831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#61384011-A-C

70323955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 61383900-T-C

70324070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61383786-G-A

70324070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61383786-G-T

70324082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383772-A-G

70324084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383770-A-G

70324121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61383753-G-A

70324121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61383753-G-C

70324121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61383753-G-T

70324668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383374-A-T

http://identifiers.org/hco/10/GRCh38#70324674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61383368-C-A

http://identifiers.org/hco/10/GRCh38#70324708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61383319-A-C

70324724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383303-C-T

70324738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383290-C-T

70324752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383277-G-A

70324752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383277-G-C

70324762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383267-A-T

70324765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383264-C-T

70324786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383238-G-A

70327092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61377000-T-C

70331772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61372441-T-C

70331801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61372412-T-C

70331851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61372354-T-C

70332156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61372065-G-A

70332255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61371956-T-C

70332863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61370935-G-T

70333252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61370566-C-T

http://identifiers.org/hco/10/GRCh38#70333779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61369926-C-A

70333879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61369841-G-A

70337020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61366326-A-G

70337067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61366284-C-G

70337395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61365956-C-T

http://identifiers.org/hco/10/GRCh38#70337495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61365845-A-C

70337514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61365821-G-A

70337548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61365799-A-G

70337599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61365776-G-T

70337803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61365597-A-T

70338219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363851-A-G

70339545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363582-C-G

70339545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363582-C-T

70339753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363435-C-T

70340224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363292-G-C

70340229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363287-C-G

70340229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363287-C-T

70340417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363127-C-T

70340420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363124-A-T

70340447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363097-G-C

70340447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363097-G-T

70340531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363009-G-T

70340533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61363007-T-A

http://identifiers.org/hco/10/GRCh38#70340542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61362998-C-A

http://identifiers.org/hco/10/GRCh38#70340555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61362984-C-A

70340555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 61362984-C-G

70340555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 61362984-C-T

70340615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61362924-A-G

70340807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61362742-T-A

70340807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61362742-T-C

70341016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61362554-G-C

70347954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61353260-G-A

70347973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61353244-C-T

70348009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61353208-G-T

70348010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61353207-C-T

70348365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61352937-A-G

70348441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61352856-T-C

http://identifiers.org/hco/10/GRCh38#70348518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#61352786-C-A

70348717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61352008-A-G

70348732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61351993-C-T

http://identifiers.org/hco/10/GRCh38#70348751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61351972-A-C

http://identifiers.org/hco/10/GRCh38#70349033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61351680-C-A

70349655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61349086-A-G

70349742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61349032-T-C

70349960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61348815-A-G

70350096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61348694-A-G

70350103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61348687-C-T

http://identifiers.org/hco/10/GRCh38#70350339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61348444-A-C

70350339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61348444-A-T

70350356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61348430-G-C

70350458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61348319-G-A

70350535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61348244-G-T

70350545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61348234-C-G

70350559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61348220-C-T

70352684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61347203-G-C

70352684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61347203-G-T

70352933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61346953-C-T

70357680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61338853-C-G

70357680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61338853-C-T

70357857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61338668-A-G

70363521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61330362-T-A

70363928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61329978-C-T

70364050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61329869-C-G

70364798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61327924-C-T

70373690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61320840-C-G

70373810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61320723-A-G

70373848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61320685-G-C

http://identifiers.org/hco/10/GRCh38#70374747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61320217-C-A

70374747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61320217-C-T

70375112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61319921-G-A

70375235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61319826-C-T

70375407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61319518-C-T

70375585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61319326-C-T

70375594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61319321-C-T

70375937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61318898-A-G

70376057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61318777-G-A

http://identifiers.org/hco/10/GRCh38#70376389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61318313-C-A

70376481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61318230-T-C

70376599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 61318110-G-A

70376599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 61318110-G-T

70376642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61318071-G-A

http://identifiers.org/hco/10/GRCh38#70376643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61318070-C-A

70376643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61318070-C-T

70376692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61318033-G-A

70376692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61318033-G-T

70376709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61318017-G-A

70376709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61318017-G-T

70376950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61317739-G-A

70377027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61317666-C-G

70377186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61317550-C-T

70377242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61317507-C-T

70377749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61315882-C-G

70377945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61315744-T-C

70377952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61315736-C-G

70377952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61315736-C-T

70378114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61315608-A-G

70378229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61315487-T-C

70378268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61315418-C-T

70380494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61313599-A-G

70380534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61313574-A-G

70380593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61313521-G-A

70380628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61313486-T-A

70380652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61313462-C-T

70380764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61313338-C-T

70381223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61312844-A-G

70381225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61312842-A-G

70381407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61312645-T-C

70381433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61312621-A-G

70381457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61312604-G-A

70381535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312525-G-A

70381535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312525-G-C

70381638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312422-T-C

http://identifiers.org/hco/10/GRCh38#70381645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61312415-C-A

70381645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312415-C-T

70381651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312409-G-T

http://identifiers.org/hco/10/GRCh38#70381667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61312385-C-A

70381667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312385-C-T

http://identifiers.org/hco/10/GRCh38#70381686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61312366-C-A

70381686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312366-C-T

70381697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312355-G-A

70381697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312355-G-T

70381716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312334-G-A

70381716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312334-G-T

70381770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312266-A-G

70381793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312243-G-T

70381823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61312213-A-T

http://identifiers.org/hco/10/GRCh38#70381910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#61312142-C-A

70381950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61312106-G-A

70381950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61312106-G-T

70382474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61311730-T-C

70382486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 61311718-A-G

70382604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61311611-G-A

70382604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23421
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 61311611-G-C