http://identifiers.org/hco/15/GRCh38#51447895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54272646-C-A

51447908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54272659-C-T

51448282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54273022-T-A

51448282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54273022-T-C

http://identifiers.org/hco/15/GRCh38#51448396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54273137-C-A

51448400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54273141-C-T

51448624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54273325-G-A

http://identifiers.org/hco/15/GRCh38#51448635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54273336-C-A

http://identifiers.org/hco/15/GRCh38#51448743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54273442-C-A

http://identifiers.org/hco/15/GRCh38#51448812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54273511-A-C

51448812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54273511-A-T

http://identifiers.org/hco/15/GRCh38#51448835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54273534-C-A

51448835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54273534-C-G

51448835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54273534-C-T

http://identifiers.org/hco/15/GRCh38#51448861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54273572-C-A

51448914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54273632-G-A

51448914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54273632-G-T

51449071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54273789-G-A

51449093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54273811-T-C

51449176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54273894-G-A

51449229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54273941-G-A

51449229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54273941-G-T

51449526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54274253-C-G

51449738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54274427-A-T

51449775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54274443-C-T

51449894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54274566-C-T

51449981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54274674-G-A

51449991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54274679-G-T

51450061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54274737-T-A

51450061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54274737-T-C

51450061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54274737-T-G

51450118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54274827-T-C

51451545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54276417-A-T

51451565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54276433-A-G

51451565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54276433-A-T

51451591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54276463-A-G

http://identifiers.org/hco/15/GRCh38#51451635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54276484-C-A

51451718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54276564-C-T

51451849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54276650-G-T

51453267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54276886-A-G

51453335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54276944-A-G

51453377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54276994-T-C

51453423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54277032-T-A

51453423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54277032-T-C

51453423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54277032-T-G

51453477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54277084-G-A

51453477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54277084-G-C

51453477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54277084-G-T

51453480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54277087-A-G

51453540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54277146-G-A

51453540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54277146-G-C

51453585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54277191-A-G

51453646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54277252-G-A

51454052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54280643-T-A

51454171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54280744-T-C

http://identifiers.org/hco/15/GRCh38#51455094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54281882-C-A

51455094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54281882-C-T

51455117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54281904-T-C

http://identifiers.org/hco/15/GRCh38#51455157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54281943-A-C

51455157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54281943-A-G

51455157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54281943-A-T

http://identifiers.org/hco/15/GRCh38#51455313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54282099-C-A

51455313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282099-C-G

51455336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282120-T-A

51455336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282120-T-C

51455854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282378-G-C

51455854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282378-G-T

51455940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282439-A-T

http://identifiers.org/hco/15/GRCh38#51455942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54282441-C-A

51455942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282441-C-T

51455979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282478-T-C

51455995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282491-C-T

51456174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54282671-G-A

51456325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54282806-G-A

51456325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282806-G-T

http://identifiers.org/hco/15/GRCh38#51456396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54282876-A-C

51456396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282876-A-G

51456495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282976-T-G

51456501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54282980-T-C

51456548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54283017-C-G

51456615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54283086-T-A

51456615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54283086-T-C

51456616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54283087-C-T

51456629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54283101-C-T

51456630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54283102-C-T

51456704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54283222-G-A

http://identifiers.org/hco/15/GRCh38#51457533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54283729-A-C

http://identifiers.org/hco/15/GRCh38#51457546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54283769-C-A

51457546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54283769-C-T

51457690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54283954-T-C

http://identifiers.org/hco/15/GRCh38#51457698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54283962-C-A

51457873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54285188-G-A

51457873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54285188-G-T

51457880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54285195-T-A

51457880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54285195-T-C

51458036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54285327-G-C

http://identifiers.org/hco/15/GRCh38#51458044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54285333-C-A

51458044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54285333-C-T

http://identifiers.org/hco/15/GRCh38#51458148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54285418-C-A

51458276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54285569-G-C

http://identifiers.org/hco/15/GRCh38#51458368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54285693-C-A

51458368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54285693-C-T

51458386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54285711-T-A

51458386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54285711-T-C

51458535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54286027-G-A

51458535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54286027-G-T

51458687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54286179-G-C

51458852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54286339-T-C

51458852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54286339-T-G

51459100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54286539-C-G

http://identifiers.org/hco/15/GRCh38#51459142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54286580-C-A

51459142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54286580-C-T

http://identifiers.org/hco/15/GRCh38#51459195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54286689-C-A

51459195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286689-C-T

51459205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286699-T-A

51459205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286699-T-C

51459205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286699-T-G

51459228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286723-G-A

51459228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286723-G-C

51459228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286723-G-T

http://identifiers.org/hco/15/GRCh38#51459261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54286753-A-C

51459261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286753-A-G

51459280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286771-G-A

51459280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286771-G-T

http://identifiers.org/hco/15/GRCh38#51459332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54286819-C-A

51459444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286925-G-C

http://identifiers.org/hco/15/GRCh38#51459455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54286936-C-A

51459455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286936-C-T

51459489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54286958-G-T

http://identifiers.org/hco/15/GRCh38#51459567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54287030-A-C

51459567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54287030-A-G

51459644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54287105-A-G

51459646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54287107-A-G

51459747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54287208-C-T

51459805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54287250-G-A

51459805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54287250-G-T

51459875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54287309-C-T

51459925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54287359-G-A

51459925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54287359-G-C

51463118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54287916-T-G

http://identifiers.org/hco/15/GRCh38#51463159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54287960-A-C

51463203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54288002-G-T

51463251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54288043-A-T

51463409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54288222-A-G

http://identifiers.org/hco/15/GRCh38#51463484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54288297-A-C

51463484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54288297-A-G

51463484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54288297-A-T

51463490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54288303-C-T

51463501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54288314-T-A

51463501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54288314-T-C

51463596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54288387-G-T

http://identifiers.org/hco/15/GRCh38#51464564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54289064-A-C

51464582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54289071-T-C

51464601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54289080-T-A

51464601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54289080-T-C

51464618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54289097-C-T

http://identifiers.org/hco/15/GRCh38#51464731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54289193-A-C

http://identifiers.org/hco/15/GRCh38#51464845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54289307-A-C

51464845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54289307-A-G

51464863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54289325-T-C

51464883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54289345-G-A

51464883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54289345-G-C

51464884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54289346-G-A

51464886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54289348-G-A

http://identifiers.org/hco/15/GRCh38#51464947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54289380-C-A

51465015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54289452-G-T

51465105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54289536-T-A

http://identifiers.org/hco/15/GRCh38#51465154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54289581-A-C

51465381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54289749-C-T

51465482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54289838-G-A

51465482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54289838-G-T

51465530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54289884-T-C

51465591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54289945-A-G

51465591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54289945-A-T

51465712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54290077-G-T

51465721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54290086-C-T

51465731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54290096-G-A

51465731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54290096-G-T

51465790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54290145-G-T

51466171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54290928-A-G

http://identifiers.org/hco/15/GRCh38#51466207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54290964-C-A

51466207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54290964-C-T

51466243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54291000-T-A

51466243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54291000-T-C

51466322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54291082-A-G

51466331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54291091-T-C

51466331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54291091-T-G

51466390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54291156-T-A

51469469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54293455-G-T

51469504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54293491-T-A

51469533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54293504-G-A

51469644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54293648-C-G

51469644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54293648-C-T

http://identifiers.org/hco/15/GRCh38#51470723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54294241-C-A

51470723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54294241-C-G

51470908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54294399-T-C

51471099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54294586-A-T

http://identifiers.org/hco/15/GRCh38#51471112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54294599-A-C

51471119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54294606-T-C

51471133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54294619-T-C

http://identifiers.org/hco/15/GRCh38#51471174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54294657-A-C

51471313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54294787-A-G

51471331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54294805-T-C

51471376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54294850-T-C

51471391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54294865-G-A

51471394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54294868-A-G

51471551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54294980-A-T

51471586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54295020-G-A

51471702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54295351-T-C

51471703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54295352-G-C

51471824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54295647-T-C

51472323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54296027-A-G

51472604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54296201-T-C

51472614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54296211-G-A

51472647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54296241-C-T

http://identifiers.org/hco/15/GRCh38#51473160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54299507-A-C

http://identifiers.org/hco/15/GRCh38#51473317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54299638-A-C

http://identifiers.org/hco/15/GRCh38#51473395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54299724-C-A

51473729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54300085-T-C

http://identifiers.org/hco/15/GRCh38#51474256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54300776-A-C

http://identifiers.org/hco/15/GRCh38#51474274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54300837-C-A

51474278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54300841-A-T

51474282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54300845-A-G

51474282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54300845-A-T

http://identifiers.org/hco/15/GRCh38#51474283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54300846-A-C

http://identifiers.org/hco/15/GRCh38#51474707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54301267-C-A

51474715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54301274-G-C

51474715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54301274-G-T

51476797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303726-G-T

51476899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303828-C-T

51477068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303957-C-G

51477068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303957-C-T

51477142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304032-A-G

51477349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304219-T-C

51478161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305216-C-T

http://identifiers.org/hco/15/GRCh38#51478187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54305244-C-A

51478187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305244-C-T

51478218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305275-A-G

51478245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305301-T-C

51478255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305311-G-A

51478255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305311-G-T

51478305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54305365-T-C

51478309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54305369-T-C

51478368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305428-A-G

51478377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305437-T-C

51478383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305443-A-G

http://identifiers.org/hco/15/GRCh38#51478395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54305455-C-A

51478395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305455-C-T

51478416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305475-T-G

51478471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305529-G-A

51478471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305529-G-C

51478471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305529-G-T

51478483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305537-T-C

51478491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305545-A-T

http://identifiers.org/hco/15/GRCh38#51478493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54305547-C-A

51479275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54306395-A-G

51479559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54306671-T-C

51479622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54306720-T-C

51479759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54306860-C-T

51480147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54307425-T-C

51480147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54307425-T-G

51480178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54307472-A-G

51480178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54307472-A-T

51480231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54307524-G-T

51480490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54308153-G-T

51480557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54308216-T-C

51480605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54308264-G-A

51480706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54308365-A-G

51480715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54308374-T-C

51480743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54308402-A-G

51480782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54308441-A-G

51480786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54308445-C-G

51480795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54308454-T-C

51480798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54308457-G-A

51480803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54308462-T-C

http://identifiers.org/hco/15/GRCh38#51480968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54308627-A-C

51481073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54308732-A-G

51481157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54308804-G-A

51481166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54308813-T-C

51481166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54308813-T-G

51481247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54308894-T-C

51481277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54308924-A-G

51486354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54311521-T-A

51486354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54311521-T-C

51486419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54311585-T-G

http://identifiers.org/hco/15/GRCh38#51486435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54311598-C-A

51486435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54311598-C-G

51486661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54311884-C-G

51486869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54312067-G-C

51487032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54312210-A-G

51487032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54312210-A-T

51487124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54312292-T-G

51487238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54312405-G-T

51487814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54312916-G-A

51487814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54312916-G-C

51487814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54312916-G-T

51487819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54312921-T-C

http://identifiers.org/hco/15/GRCh38#51488403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54313733-C-A

51488403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54313733-C-T

51488439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54313769-G-A

51488439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54313769-G-T

http://identifiers.org/hco/15/GRCh38#51488535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54313868-C-A

51488586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54313919-A-G

http://identifiers.org/hco/15/GRCh38#51488730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54314063-C-A

51488749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54314080-T-C

51488750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54314081-G-T

51488960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54314243-A-T

51491881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54316732-T-A

http://identifiers.org/hco/15/GRCh38#51491894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54316745-C-A

51492038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54317031-T-C

51494257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54318017-A-G

51494280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54318034-G-T

51494320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54318069-T-C

51494338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54318086-A-G

51494423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54318173-C-T

51494934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54318796-T-A

51494934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54318796-T-C

51495156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319016-T-A

51495156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319016-T-C

http://identifiers.org/hco/15/GRCh38#51495285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54319153-C-A

51495285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319153-C-G

51495285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319153-C-T

51495491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319703-C-T

51495567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319780-T-G

51495604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319812-T-C

51495710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319909-G-A

51496450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320266-G-C

51496471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320283-T-G

51496725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320557-G-T

51497270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321286-G-T

51497449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321483-G-T

51498435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 54322601-T-A

http://identifiers.org/hco/15/GRCh38#51498442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54322610-C-A

51498442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 54322610-C-G

51498442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54322610-C-T

51498489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54322654-A-G

51498489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54322654-A-T

51498589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54322751-A-G

51498598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54322760-A-G

51498610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54322772-A-G

51498718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54322880-T-C

51499242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54323404-T-C

51499275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54323437-T-C

51499378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54323534-G-A

51499378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54323534-G-T

51500046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54324202-C-G

51500295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54324445-T-C

http://identifiers.org/hco/15/GRCh38#51501359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54325418-C-A

51501359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54325418-C-T

51502816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54327039-C-T

51503132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54327340-T-G

51506895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54328473-A-T

http://identifiers.org/hco/15/GRCh38#51507064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54330438-C-A

51507064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54330438-C-T

51507090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54330465-A-G

51507124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54330504-A-G

51515396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54333868-A-G

51515450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54333920-G-A

51515629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54334245-C-T

51515647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54334263-C-T

51515677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54334309-C-T

http://identifiers.org/hco/15/GRCh38#51515991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54334551-C-A

51516086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54334644-A-G

51516256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54334773-G-A

51516475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54334980-T-C

51516519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54335026-T-C

51517003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54335235-G-T

http://identifiers.org/hco/15/GRCh38#51517123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54335363-A-C

51517195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54335435-T-C

51517240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54335480-G-T

51517274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54335508-G-A

51517274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54335508-G-T

51517479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54335702-G-C

51517763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54335923-T-C

51519545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54337655-G-C

51521321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54342720-T-A

51521682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54342922-T-A

51521682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54342922-T-C

51522030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54343271-T-A

51522732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54343798-C-G

51522732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54343798-C-T

51522743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54343809-T-A

51523107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54344181-A-G

51523393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54344418-A-G

51534463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54350697-T-C

51534835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54351144-T-C

51534851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54351160-C-T

51534883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54351192-C-T

51535132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54351921-T-C

51535543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54352560-T-C

51535543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54352560-T-G

http://identifiers.org/hco/15/GRCh38#51535549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54352566-C-A

http://identifiers.org/hco/15/GRCh38#51535568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54352586-C-A

51535568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54352586-C-T

51535591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54352608-A-G

51535591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54352608-A-T

51536154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54353644-A-G

51536154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54353644-A-T

51536415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54353905-A-G

51536425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54353915-T-G

51536539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54354029-G-A

51536542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54354032-A-G

51536654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54354144-G-A

51536783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54354270-G-C

51536917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54354413-A-G

51536969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54354493-T-C

51537257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54354871-T-C

51537336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54354942-T-A

http://identifiers.org/hco/15/GRCh38#51537376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54354977-C-A

51537398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54354999-G-A

51537398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54354999-G-C

51537398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54354999-G-T

51537435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54355037-T-C

51537451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54358043-T-C

http://identifiers.org/hco/15/GRCh38#51537468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54358060-A-C

51537468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54358060-A-G

http://identifiers.org/hco/15/GRCh38#51537614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54358207-C-A

51537614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54358207-C-G

51537614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54358207-C-T

http://identifiers.org/hco/15/GRCh38#51538250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54358923-C-A

51538250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54358923-C-G

51538250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54358923-C-T

http://identifiers.org/hco/15/GRCh38#51538508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54359186-C-A

51538508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54359186-C-T

51538544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54359227-G-A

51538544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54359227-G-T

51538828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54359512-A-G

51540691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54360554-T-C

51540956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54360905-A-T

51541063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54361011-G-A

51541063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54361011-G-C

51541402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54364114-T-C

51541471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54364183-C-G

51541474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54364186-C-T

51542020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54364646-T-A

51542067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54364692-C-T

51542095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54364720-T-C

51542196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54364804-A-G

51542196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54364804-A-T

51542302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54364889-T-C

51542397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54364972-G-A

51542550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54365125-T-C

51545252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54365892-T-C

51545290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54365933-G-A

51545535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54366094-G-T

51545547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54366105-T-C

51545637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54366192-G-A

51545642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54366197-T-C

http://identifiers.org/hco/15/GRCh38#51545786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54366341-A-C

51545818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54366373-A-G

http://identifiers.org/hco/15/GRCh38#51545819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54366374-C-A

51545819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54366374-C-T

http://identifiers.org/hco/15/GRCh38#51545916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54366464-A-C

51546081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54366592-A-G

51547041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54368041-C-T

http://identifiers.org/hco/15/GRCh38#51547086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54368081-C-A

51547320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54368313-T-C

http://identifiers.org/hco/15/GRCh38#51547419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54368412-C-A

51547419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54368412-C-T

51547423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54368416-G-A

51547423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54368416-G-C

51547423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54368416-G-T

51547622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54368772-A-T

51547919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54369024-G-T

51550819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54370733-G-A

51550941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54370845-A-T

51551139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54371033-A-T

51554489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54372709-T-G

http://identifiers.org/hco/15/GRCh38#51557748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54375458-A-C

51557783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54375490-T-A

51557925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54375624-A-T

51558385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

51558385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

51559908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54378354-A-G

51563355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54379453-T-C

51563969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54380019-A-G

51564012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54380069-G-A

51564012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54380069-G-T

51564049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54380104-T-A

51564049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54380104-T-C

51564104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54380151-A-T

51564167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54380214-A-T

51564175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54380222-A-G

51564178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54380225-A-G

51564238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54380285-A-G

http://identifiers.org/hco/15/GRCh38#51564382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54380425-C-A

51564382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54380425-C-T

51564401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54380443-A-T

51564446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54380496-A-G

51564855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54380892-C-T

51565076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54381109-A-G

http://identifiers.org/hco/15/GRCh38#51565137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54381170-C-A

51565137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54381170-C-T

http://identifiers.org/hco/15/GRCh38#51565226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54381245-C-A

51565226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54381245-C-T

http://identifiers.org/hco/15/GRCh38#51565310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54381322-C-A

51565456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54381452-C-T

http://identifiers.org/hco/15/GRCh38#51566911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54383799-C-A

51566999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54383880-T-G

51567026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54383915-T-C

51568167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54384398-T-C

51568168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54384399-G-T

http://identifiers.org/hco/15/GRCh38#51568238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54384464-C-A

51568289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54384511-T-C

51568298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54384520-G-A

51568358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54384540-C-T

51568400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54384576-T-C

51568579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54384833-C-T

51568612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54384866-T-A

51568631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54384885-G-A

51568631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54384885-G-T

http://identifiers.org/hco/15/GRCh38#51568657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54384911-A-C

51568704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54384958-T-A

51574132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54385584-T-C

51574325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54385767-T-C

51574936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54386517-C-T

51575008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54386612-C-T

51575242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54386822-G-A

51575242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54386822-G-C

51575418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54386988-T-C

51575820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54387476-G-C

51575883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54387537-G-T

51575930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54387575-C-T

51575934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54387579-T-C

51576025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54387593-T-C

51576025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54387593-T-G

http://identifiers.org/hco/15/GRCh38#51576303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54387864-C-A

51576445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54388332-G-A

51576491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54388374-T-C

http://identifiers.org/hco/15/GRCh38#51576529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54388423-A-C

51580272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54390511-C-G

51580281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54390515-C-T

51580282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54390516-G-A

51580285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54390519-A-G

51580320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54390550-G-A

51580320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54390550-G-T

51580329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54390559-T-C

51586228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54395708-T-G

51586556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54396269-G-T

51616156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54400993-T-A

51616219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54401071-T-C

51616220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54401072-T-C

51616339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54401136-C-T

http://identifiers.org/hco/15/GRCh38#51616351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54401139-C-A

51616351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54401139-C-T

51616363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54401151-A-G

51617830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54402777-C-T

51618369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54403434-G-A

51618504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54403862-T-A

51618626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54404091-A-G

51618627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54404092-T-A

51618822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54404276-C-T

51619002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54404452-G-C

51619068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54404529-T-C

51619425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54405140-G-C

51619513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54405222-G-A

51619795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54405497-T-C

51619970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54405659-C-T

51620434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54406433-G-A

51620463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54406476-G-A

51620507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54406518-A-G

51620696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54406712-T-C

51620836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54406822-C-T

51620922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54406903-G-A

51620991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54407076-A-G

51621043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54407122-G-A

51621065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54407143-G-C

51621144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54407254-T-C

51621645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54408015-T-G

51621826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54408212-C-G

http://identifiers.org/hco/15/GRCh38#51622086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54408385-C-A

http://identifiers.org/hco/15/GRCh38#51622363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54408603-A-C

http://identifiers.org/hco/15/GRCh38#51622470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#54408646-C-A

51622470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54408646-C-G

51622470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54408646-C-T

51622600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 54408777-G-A

51622600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 54408777-G-C

http://identifiers.org/hco/15/GRCh38#51622740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54408872-C-A

51622740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 54408872-C-G

51622740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 54408872-C-T

51622825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 54408958-G-A

51622825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 54408958-G-C

51622825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2938
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 54408958-G-T