46549594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061682-C-G

46549594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061682-C-T

46549738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061435-T-C

46549747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061427-G-T

46549760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061414-G-A

46549767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061407-A-G

46549797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061377-C-T

46549801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061373-T-A

46549813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061362-T-C

46549858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061315-A-G

46549928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061250-A-G

46550099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061080-A-G

46550132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44061054-T-C

46550418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44060812-C-T

46550458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44060772-G-A

46550584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44060645-A-G

46550725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44060500-C-G

46550725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44060500-C-T

46552355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44058991-T-G

46552601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44058072-T-C

http://identifiers.org/hco/6/GRCh38#46552650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44058038-C-A

46553675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44057589-G-A

46553675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44057589-G-C

46553675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44057589-G-T

46553709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44057558-G-T

46553739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44057529-T-C

46553798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44057470-T-C

http://identifiers.org/hco/6/GRCh38#46553873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44057395-A-C

http://identifiers.org/hco/6/GRCh38#46554003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44057356-C-A

46554003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44057356-C-T

46563008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44057073-G-T

46563017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44057064-A-G

46563102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44056962-T-A

http://identifiers.org/hco/6/GRCh38#46563152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44056925-C-A

46563152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44056925-C-T

46563252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44056850-A-G

46563258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44056844-G-A

46563258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44056844-G-T

46563260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44056842-A-G

http://identifiers.org/hco/6/GRCh38#46563519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44056543-A-C

46563831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44056247-G-A

46563895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44056184-A-G

46563905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44056170-G-A

46563948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44056132-G-A

http://identifiers.org/hco/6/GRCh38#46564708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44055635-C-A

46564708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44055635-C-T

46564774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44055569-C-G

46564774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44055569-C-T

46564989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44055344-A-G

46565011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44055331-C-G

46565011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44055331-C-T

46565036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44055311-C-T

46565165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44055181-T-C

46565167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44055179-G-A

46565197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44055151-G-T

46565360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44054999-T-C

46565392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44054970-T-C

http://identifiers.org/hco/6/GRCh38#46565428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44054934-A-C

46565428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44054934-A-T

46565431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44054931-T-A

46565431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44054931-T-G

46565456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44054906-T-A

46565456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44054906-T-C

http://identifiers.org/hco/6/GRCh38#46565460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44054902-C-A

46565460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44054902-C-T

46565464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44054898-A-T

46574618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44048227-G-A

46582610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44047222-C-T

http://identifiers.org/hco/6/GRCh38#46582661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44047171-A-C

46582661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44047171-A-G

46583297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44046021-A-G

46583297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44046021-A-T

46583325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44045993-C-T

http://identifiers.org/hco/6/GRCh38#46583415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44045930-C-A

46583415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44045930-C-T

46583427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44045918-A-G

http://identifiers.org/hco/6/GRCh38#46583449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44045900-C-A

http://identifiers.org/hco/6/GRCh38#46583453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44045898-C-A

46583453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44045898-C-T

http://identifiers.org/hco/6/GRCh38#46583463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/17/GRCm39#44045888-C-A

46583504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44045847-T-C

46583508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44045843-G-A

46583508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44045843-G-T

46583574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44045777-T-A

46583621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44045707-C-G

46583627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44045701-G-A

46583627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44045701-G-T

46583899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44045362-T-C

46583915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44045346-A-T

http://identifiers.org/hco/6/GRCh38#46583917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44045344-C-A

46584001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44045260-A-G

46584966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44044250-G-A

46584981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44044235-A-G

46584981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44044235-A-T

46585163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44044059-A-G

46586961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44043007-G-A

46586961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44043007-G-T

46587009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042969-T-C

http://identifiers.org/hco/6/GRCh38#46587037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44042942-C-A

46587037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042942-C-T

46587039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042940-G-C

46587039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042940-G-T

46587056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042923-T-C

46587067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042912-T-A

46587067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042912-T-C

46587098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44042881-C-T

http://identifiers.org/hco/6/GRCh38#46587192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44042787-C-A

46587192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042787-C-T

http://identifiers.org/hco/6/GRCh38#46587232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44042749-A-C

46587268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042713-A-G

46587486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042494-A-G

46587498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042482-G-A

46587560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042420-T-C

46587625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042357-G-A

46587625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042357-G-T

46587777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042206-A-T

46587779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042204-C-T

46587875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042114-T-C

46587890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042099-G-T

46587932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042057-G-A

46587932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042057-G-T

46587943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042046-T-C

46587943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042046-T-G

http://identifiers.org/hco/6/GRCh38#46587977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44042012-C-A

46587977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44042012-C-T

46587989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44041997-G-A

46587989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44041997-G-T

46588213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44041776-T-A

46588213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44041776-T-G

46593792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44040484-T-C

46594065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44038585-A-G

46594115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44038544-A-G

46594120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44038540-G-T

46594134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44038526-A-G

http://identifiers.org/hco/6/GRCh38#46594313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44038343-A-C

46594415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44038212-T-C

46594488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44038149-A-G

46594611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44038028-A-T

46594891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44037773-T-C

46594933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44037731-T-C

46595159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44037360-T-C

46595272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44037246-A-G

46595383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44037067-A-G

46595406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44037044-T-C

46595848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44036666-T-C

http://identifiers.org/hco/6/GRCh38#46595853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44036661-C-A

46595853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44036661-C-T

46595937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44036586-G-A

46595956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44036569-T-C

http://identifiers.org/hco/6/GRCh38#46595991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44036533-A-C

46596148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44036373-A-G

46596168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44036353-A-G

46596214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44036314-G-A

46596214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44036314-G-T

46596227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44036301-G-C

46596227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44036301-G-T

46596436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44036165-A-G

46596456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44036145-C-T

46596739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44034142-G-C

46596818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44034086-T-C

46596907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44033997-T-G

46596913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44033991-C-G

46601944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44029862-A-G

46602104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44029704-C-G

46602123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44029685-C-G

46602212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44029608-G-T

46602248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44029571-T-C

46602750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44029263-C-T

46603529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44028476-C-T

http://identifiers.org/hco/6/GRCh38#46604005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44028054-C-A

46604071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44028027-A-G

46604119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44027994-G-A

46604178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44027941-A-G

46604265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44027860-C-T

46604435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44027686-G-A

46605704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44026669-G-A

46605709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44026664-G-A

http://identifiers.org/hco/6/GRCh38#46605786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44026584-A-C

46606047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44025741-A-G

46606193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44025582-C-T

http://identifiers.org/hco/6/GRCh38#46606456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44025344-A-C

46606668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44025139-T-G

46606745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44025045-T-C

http://identifiers.org/hco/6/GRCh38#46606867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44024932-A-C

46607118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44022850-G-A

46607118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44022850-G-T

46607130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44022841-C-T

http://identifiers.org/hco/6/GRCh38#46607141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44022831-A-C

46607141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44022831-A-G

46607141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44022831-A-T

46607192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44022778-G-A

http://identifiers.org/hco/6/GRCh38#46607439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44022496-C-A

46607440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44022495-T-A

46607608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44021447-T-C

http://identifiers.org/hco/6/GRCh38#46607626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44021429-A-C

46608081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44021000-C-T

http://identifiers.org/hco/6/GRCh38#46612370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44018872-A-C

46612393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44018850-G-A

46612425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44018823-G-A

46612425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44018823-G-T

46612580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44018689-G-C

http://identifiers.org/hco/6/GRCh38#46612757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44018519-C-A

46612805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44018471-G-A

http://identifiers.org/hco/6/GRCh38#46613022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44018287-A-C

46613093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44018220-T-C

http://identifiers.org/hco/6/GRCh38#46613127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44018186-A-C

46613218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44018121-C-T

46613270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44018089-T-C

46613285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44018076-T-C

http://identifiers.org/hco/6/GRCh38#46613683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44017240-C-A

46613690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44017234-A-G

http://identifiers.org/hco/6/GRCh38#46613729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44017191-C-A

46613736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44017184-T-C

46613737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44017183-G-A

http://identifiers.org/hco/6/GRCh38#46613798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44017123-C-A

46613807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44017114-G-C

http://identifiers.org/hco/6/GRCh38#46613881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44017038-C-A

46613913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44017007-T-A

46613938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44016983-G-A

46613938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44016983-G-C

46613938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44016983-G-T

http://identifiers.org/hco/6/GRCh38#46613974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44016949-C-A

46613974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44016949-C-T

46614039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44016900-A-G

46614103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44016716-C-T

46614156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44016659-G-A

http://identifiers.org/hco/6/GRCh38#46624027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44013569-A-C

46624295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44013190-T-C

46624296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44013189-T-C

46624313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44013106-T-G

46624330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44013058-A-G

46624377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44013010-A-G

46624475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44012907-G-A

46624475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44012907-G-T

46624601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44012790-T-C

http://identifiers.org/hco/6/GRCh38#46625374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44012490-C-A

46625374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44012490-C-T

http://identifiers.org/hco/6/GRCh38#46625387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44012477-C-A

http://identifiers.org/hco/6/GRCh38#46625509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44012365-C-A

46625509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 44012365-C-T

46625527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44012347-T-C

46625527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44012347-T-G

46625764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44011886-C-T

46625802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44011845-T-C

46625802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44011845-T-G

http://identifiers.org/hco/6/GRCh38#46626573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44010350-C-A

http://identifiers.org/hco/6/GRCh38#46626614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44010315-A-C

46626770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44010205-C-G

46626815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44010162-T-G

46626852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44010125-A-T

46627800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44009103-G-C

46628020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44008905-A-G

46628134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44008795-T-C

46628522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44007821-T-C

46628646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44007684-T-C

http://identifiers.org/hco/6/GRCh38#46628705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44007628-A-C

46628706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44007627-C-T

http://identifiers.org/hco/6/GRCh38#46628709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44007624-C-A

46628980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44005265-G-T

46629301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44004981-G-T

46629364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44004921-T-C

46629451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44004859-T-C

http://identifiers.org/hco/6/GRCh38#46629489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44004824-C-A

46629525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44004800-A-G

46629819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44004529-T-C

46629926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44004460-G-T

46630228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44003711-G-A

46630229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44003710-A-G

46630479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44003483-T-C

46630483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44003479-G-A

46630859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44002766-T-A

46630859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44002766-T-C

46630871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44002754-A-G

46630871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44002754-A-T

http://identifiers.org/hco/6/GRCh38#46630896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44002693-A-C

46630896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44002693-A-G

46630945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44002644-C-T

46631034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44002559-C-T

46631106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44002489-T-A

46631106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44002489-T-C

46631111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44002484-G-T

46631119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44002476-T-A

46631119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44002476-T-C

http://identifiers.org/hco/6/GRCh38#46631146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#44002449-C-A

46631146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44002449-C-T

46635964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43997603-T-A

46635968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43997599-T-C

46636210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43996320-C-T

46636268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43996271-G-T

46636315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43996234-T-C

46636339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43996211-T-C

46636342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43996208-T-C

46636380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43996174-A-G

46636380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43996174-A-T

46636529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43996026-G-A

46636535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43996022-A-T

http://identifiers.org/hco/6/GRCh38#46636537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#43996020-A-C

46636537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43996020-A-G

46636550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43996007-A-G

46636625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995929-T-A

46636724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995833-G-C

46636789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995777-G-T

46636837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995732-G-A

46636889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995674-T-C

46636889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995674-T-G

46637035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995569-T-C

46637097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43995511-T-G

http://identifiers.org/hco/6/GRCh38#46637238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#43995437-C-A

46637238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995437-C-T

46637239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995436-C-G

46637250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995425-G-A

46637277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43995397-T-C

46637302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995373-C-G

46637419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43995266-G-A

46637512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995206-C-T

46637585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995149-A-T

46637600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43995134-C-T

46637643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43994944-G-A

46637776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43994025-G-T

http://identifiers.org/hco/6/GRCh38#46637888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/17/GRCm39#43993927-A-C

http://identifiers.org/hco/6/GRCh38#46637931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#43993884-A-C

46637946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: missense variant
orthologous variants: 43993869-A-G

http://identifiers.org/hco/6/GRCh38#46638276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#43992354-C-A

46638374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43992276-G-A

http://identifiers.org/hco/6/GRCh38#46638387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#43992263-C-A

46638387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43992263-C-T

46638859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43991732-T-C

46638932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43991658-C-T

46639117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43991477-T-C

46639139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43991471-T-C

http://identifiers.org/hco/6/GRCh38#46639213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#43991404-A-C

46639231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43991386-C-T

46639426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43991230-T-C

46639485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43991196-T-C

46639553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 43991128-T-C

46639628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 43991053-T-C

46639630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant
orthologous variants: 43991051-T-G

46639632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, missense_variant
orthologous variants: 43991049-T-C

46639676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 43991005-C-T

http://identifiers.org/hco/6/GRCh38#46639679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#43991002-A-C

46639702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43990979-A-G

46639787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43990923-G-A

46639787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43990923-G-T

46640875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43989013-C-T

46641112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43988891-A-G

46641464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43988556-G-A

46641648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43988354-T-A

46641718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43988274-C-T

46641824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43988178-T-C

46641829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43988173-C-T

46641942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43988073-C-T

46642017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43988000-C-T

46642019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43987998-C-T

46642061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43987956-C-T

46642347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43987661-G-A

46642347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43987661-G-C

46642347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43987661-G-T

46642361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43987646-T-A

46642436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43987110-T-G

46642555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43986882-T-G

46642614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43986841-C-T

46643772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -G-A

46643789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -T-G

46643842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -G-A

46643889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -T-C

46644260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -T-G

46644410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -T-C

46645079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -T-G

46645433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -G-C

46645441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -T-G

46645460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -T-G

46645500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -C-T

46645560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -A-G

46645568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -T-A

46645584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -C-T

46645592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -T-C

46645609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: -C-G

46649986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43981958-T-C

46649988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43981956-T-C

46649995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43981949-G-A

46650914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43980881-A-G

46651113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43980683-A-G

46651113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43980683-A-T

46651774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43979281-C-T

46651779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43979276-A-G

46651962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43979055-A-G

46652307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43978772-T-A

46652307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: intron variant
orthologous variants: 43978772-T-C

http://identifiers.org/hco/6/GRCh38#46652482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#43978607-C-A

46652517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 43978572-C-T

46652609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: 43978486-A-G

http://identifiers.org/hco/6/GRCh38#46652656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#43978433-C-A

46652656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: 43978433-C-G

46652656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: 43978433-C-T

46652698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: 43978387-T-C

http://identifiers.org/hco/6/GRCh38#46652740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#43978341-A-C

46652740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: 43978341-A-G

46652740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: 43978341-A-T

46652779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: 43978300-T-C

46652824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: 43978233-G-A

46652824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: 43978233-G-T

http://identifiers.org/hco/6/GRCh38#46652828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#43978229-C-A

46652828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: 43978229-C-G

46652828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17449
most severe consequence: 5 prime UTR variant
orthologous variants: 43978229-C-T