67821078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86450265-G-A

http://identifiers.org/hco/4/GRCh38#67821118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86450302-C-A

67821176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86450480-A-G

67821191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86450494-T-A

67821191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86450494-T-C

67821244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86450604-A-G

67821570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86450954-G-T

67821621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86451003-G-A

67821703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86451099-T-G

67821920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86451174-T-C

67821921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86451175-T-C

67821941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86451184-G-C

67821941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86451184-G-T

http://identifiers.org/hco/4/GRCh38#67822135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86451267-C-A

67822141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86451273-T-G

67822146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86451278-T-C

http://identifiers.org/hco/4/GRCh38#67822275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86451404-C-A

67822275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86451404-C-T

67822304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86451433-T-C

67822323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86451454-A-G

http://identifiers.org/hco/4/GRCh38#67822366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86451499-C-A

67822366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86451499-C-T

67822509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451641-A-T

67822592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451715-A-T

67822593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451716-T-C

http://identifiers.org/hco/4/GRCh38#67822638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86451746-A-C

67822638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451746-A-G

67822644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451752-T-C

67822827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451907-T-G

67822836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451916-G-C

67823041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452046-T-A

http://identifiers.org/hco/4/GRCh38#67823195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86452212-A-C

67823546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452577-G-A

http://identifiers.org/hco/4/GRCh38#67823589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86452615-C-A

67823824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452842-G-T

67823867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452891-C-T

http://identifiers.org/hco/4/GRCh38#67823884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86452908-A-C

67823949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452962-C-T

http://identifiers.org/hco/4/GRCh38#67824083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86453066-C-A

67824142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86453124-T-G

http://identifiers.org/hco/4/GRCh38#67825541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86453937-A-C

67825702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86454104-A-T

67825758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86454152-G-A

67825993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86454385-G-C

67825993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86454385-G-T

67826025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86454417-A-G

67826025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86454417-A-T

http://identifiers.org/hco/4/GRCh38#67826428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86455928-A-C

http://identifiers.org/hco/4/GRCh38#67826736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86456265-C-A

67827213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86457071-C-T

67827415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 86457277-A-G

67827427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 86457289-G-A

http://identifiers.org/hco/4/GRCh38#67827542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86457423-C-A

67831476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86471701-G-A

67831476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86471701-G-C

67832220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472421-T-C

67832263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472469-T-C

67832860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86473911-A-T

67833020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474063-A-T

67833121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474170-A-G

67833161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474224-C-G

67833183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474246-G-A

67833183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474246-G-T

67833186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474249-A-G

67833196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 86474259-G-T

67833362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86474425-G-C

67833409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86474500-G-A

http://identifiers.org/hco/4/GRCh38#67833430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86474520-A-C

67834089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474598-C-T

67834102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474611-G-A

67834193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474709-A-G

67834288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474789-A-G

67834320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474826-C-T

67834572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475083-C-G

67834711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475217-G-T

67834848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475353-G-A

67834985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475432-T-C

67835102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 86475496-T-C

67835162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475563-C-T

67835176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475578-C-T

67835178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475580-A-G

67835198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475600-A-G

67835414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475809-A-T

67836137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86476461-C-G

67836147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86476471-T-C

67836147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86476471-T-G

67836413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86476683-C-T

67836569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86476851-A-G

67837211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86477563-C-T

67837388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86477910-G-A

67837652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86478155-T-G

67838069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86478833-T-A

67838119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86478879-G-A

67838119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86478879-G-T

67838317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86479072-A-T

http://identifiers.org/hco/4/GRCh38#67838318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86479073-C-A

67838318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86479073-C-G

67838318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86479073-C-T

67838430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86479169-T-C

67838458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86479185-G-A

67838458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86479185-G-T

http://identifiers.org/hco/4/GRCh38#67838460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86479187-A-C

67838460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86479187-A-G

67838476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86479199-G-A

67838476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86479199-G-T

http://identifiers.org/hco/4/GRCh38#67838635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86479356-C-A

67838635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86479356-C-G

67838722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86479441-T-C

67838722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86479441-T-G

67838887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86479600-C-T

67841272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86483889-C-G

67841283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86483900-C-G

67841426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86484016-A-G

67841750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86484322-T-A

67841906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86484438-G-T

67841940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86484472-G-A

http://identifiers.org/hco/4/GRCh38#67842174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86484715-A-C

67842174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86484715-A-G

http://identifiers.org/hco/4/GRCh38#67842279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86484811-A-C

67842284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86484816-G-A

67842284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86484816-G-T

67842300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86484832-T-C

67842536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86485063-T-A

http://identifiers.org/hco/4/GRCh38#67842664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86485193-C-A

67842664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86485193-C-T

67842695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86485222-A-T

67842701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86485229-A-T

67842713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86485242-G-A

67842713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86485242-G-T

67842829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86485352-T-C

67844218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86485747-A-G

http://identifiers.org/hco/4/GRCh38#67845902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86486118-C-A

67846105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86486274-G-A

http://identifiers.org/hco/4/GRCh38#67846171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86486348-A-C

http://identifiers.org/hco/4/GRCh38#67854104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86486676-C-A

67854104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 86486676-C-T

67854205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86486776-G-A

67854205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86486776-G-T

67859504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86487300-T-C

67859784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86487556-A-G

67859784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86487556-A-T

http://identifiers.org/hco/4/GRCh38#67859792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86487564-A-C

67859792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86487564-A-G

http://identifiers.org/hco/4/GRCh38#67859809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86487581-C-A

67859809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86487581-C-T

67859837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86487614-C-T

67859849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86487626-G-A

67859852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86487629-T-C

67860009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86487950-A-G

67860009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86487950-A-T

67860127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86488061-A-G

67860294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86488405-C-T

67860448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86488612-G-T

67860459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86488623-C-G

67860517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86488686-A-G

67860563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86488725-A-G

67860576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86488736-A-G

67860596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86488752-T-C

67860661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86488806-T-C

67860716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86488862-C-T

http://identifiers.org/hco/4/GRCh38#67861053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86489175-C-A

67861484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86489591-T-G

67861653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86491729-A-T

67861836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86491913-T-C

67861907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86491966-G-A

67861936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86492017-T-C

67861967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86492053-A-T

67862159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86492209-A-T

67862168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86492218-T-C

67862295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86492335-C-T

http://identifiers.org/hco/4/GRCh38#67862332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86492367-C-A

67862332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86492367-C-G

67862356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86492391-A-G

67869226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86497694-T-G

67869391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86497793-A-T

67872712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86503275-G-T

67873299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86503849-C-T

67873371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86503890-C-T

67873662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86504208-A-T

67873670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86504216-A-G

67873784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86504310-A-G

67873829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86504355-A-G

67873869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86504389-C-T

67874325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86504490-A-G

67874604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86504821-G-A

67874604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86504821-G-C

67874736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86504948-T-G

67874818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86505015-G-T

67874944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86505140-A-G

67875155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86505307-C-G

http://identifiers.org/hco/4/GRCh38#67875157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86505309-A-C

67875157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86505309-A-G

67875212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86505368-C-T

67875409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86505534-T-C

67875599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86505821-C-G

67875637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86505874-T-C

http://identifiers.org/hco/4/GRCh38#67875649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86505886-C-A

67875752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86505981-A-G

67876112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86506312-G-A

67876277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86506466-C-T

67876377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86506526-A-G

http://identifiers.org/hco/4/GRCh38#67876389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86506538-C-A

http://identifiers.org/hco/4/GRCh38#67876442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86506577-A-C

67876564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86506887-G-T

67876660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86506979-C-T

67877241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86507649-T-A

67877361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86507754-G-A

67877448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86507816-G-A

67877634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86508012-T-C

67881257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86518909-G-A

http://identifiers.org/hco/4/GRCh38#67881625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86519214-C-A

67881634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86519223-G-A

http://identifiers.org/hco/4/GRCh38#67881790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86519371-A-C

67881860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86519442-T-C

67882035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86519619-T-C

67882151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86519760-T-C

67883021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86520314-A-G

67883049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86520340-A-G

67883295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86520557-G-A

67883301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86520566-G-A

67883301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86520566-G-T

67883634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86520901-G-A

67883654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86520921-C-T

67883687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86520953-G-A

67883774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86521056-T-G

http://identifiers.org/hco/4/GRCh38#67883775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86521057-A-C

67883775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86521057-A-G

67883789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86521071-A-G

67883789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86521071-A-T

http://identifiers.org/hco/4/GRCh38#67883799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86521081-A-C

67883816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86521098-A-G

67883859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86521139-T-C

67883909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86521187-A-G

67883910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86521188-C-T

67883951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86521232-A-G

67883951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24059
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86521232-A-T