http://identifiers.org/hco/11/GRCh38#6621332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105402203-C-A

6621425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 3 prime UTR variant
orthologous variants: 105402289-G-A

6621425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 3 prime UTR variant
orthologous variants: 105402289-G-T

http://identifiers.org/hco/11/GRCh38#6621457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105402316-C-A

6621457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105402316-C-T

http://identifiers.org/hco/11/GRCh38#6621463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105402323-A-C

6621463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105402323-A-G

6621836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105402722-T-C

http://identifiers.org/hco/11/GRCh38#6622336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105403222-C-A

6622336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105403222-C-T

http://identifiers.org/hco/11/GRCh38#6622517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#105403403-C-A

6622517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous_variant, undefined
orthologous variants: 105403403-C-T

http://identifiers.org/hco/11/GRCh38#6622550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105403436-A-C

6622550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105403436-A-G

6622739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105403625-T-C

6622739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105403625-T-G

6622931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105403817-T-C

6622931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105403817-T-G

6622990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105403876-G-A

6622990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105403876-G-C

6622990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105403876-G-T

6623174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105404060-G-A

6623174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105404060-G-T

http://identifiers.org/hco/11/GRCh38#6623396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105404282-C-A

6623396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105404282-C-T

http://identifiers.org/hco/11/GRCh38#6623457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105404343-C-A

6623457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105404343-C-T

http://identifiers.org/hco/11/GRCh38#6623489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105404375-A-C

6623489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105404375-A-G

6623549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105404435-G-A

6623550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105404436-T-A

6623665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105404551-C-G

6623665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105404551-C-T

6623708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105404594-T-A

6624200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105405086-A-G

6624275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105405161-T-C

6624275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105405161-T-G

6624290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105405176-C-T

6624452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105405339-T-C

6624484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105405371-A-G

http://identifiers.org/hco/11/GRCh38#6624675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105405562-C-A

6624794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105405683-G-T

http://identifiers.org/hco/11/GRCh38#6624929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105405818-C-A

http://identifiers.org/hco/11/GRCh38#6624955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105405846-C-A

6624955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105405846-C-T

http://identifiers.org/hco/11/GRCh38#6625066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105405949-C-A

6625139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105406045-C-T

6625269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105406177-G-A

6625269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105406177-G-C

http://identifiers.org/hco/11/GRCh38#6625559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105406452-C-A

6625559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105406452-C-T

6625655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105406531-G-A

6625840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105406719-G-A

http://identifiers.org/hco/11/GRCh38#6625845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105406724-C-A

6626438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105407305-C-G

http://identifiers.org/hco/11/GRCh38#6626510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105407333-C-A

6626510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105407333-C-T

6626758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105407571-C-T

http://identifiers.org/hco/11/GRCh38#6626828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105407641-C-A

6626828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105407641-C-T

6626883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105407696-A-G

6627084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105407897-T-C

6627084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105407897-T-G

6627164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105407977-T-C

6627393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105408206-A-G

6628104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105408887-G-T

6628404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105409805-G-T

http://identifiers.org/hco/11/GRCh38#6628763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105410163-A-C

6628772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105410172-A-G

http://identifiers.org/hco/11/GRCh38#6628890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105410289-C-A

6628890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105410289-C-T

6629440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105410752-G-A

6629477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105410787-C-T

6629501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105410811-C-T

6629585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105410895-G-T

6629656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105410966-C-G

6629656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105410966-C-T

6629665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105411003-G-A

6629665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105411003-G-C

6629766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105411104-A-G

6629937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron variant
orthologous variants: 105411273-T-C

6630201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105411543-T-C

6630306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105411648-G-A

6630381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous_variant, undefined
orthologous variants: 105411723-G-A

6630381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense_variant, undefined
orthologous variants: 105411723-G-C

6630381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense_variant, undefined
orthologous variants: 105411723-G-T

6630461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105411803-G-A

6630461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense variant
orthologous variants: 105411803-G-T

http://identifiers.org/hco/11/GRCh38#6630465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105411807-C-A

6630465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: synonymous variant
orthologous variants: 105411807-C-T

6630519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105411861-T-G

http://identifiers.org/hco/11/GRCh38#6630576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#105411918-C-A

6630576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 105411918-C-G

6630576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 105411918-C-T

6630712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 105412054-C-T

6630747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105412089-A-T

6630762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105412104-T-C

http://identifiers.org/hco/11/GRCh38#6630770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105412112-C-A

6630770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105412112-C-T

http://identifiers.org/hco/11/GRCh38#6630786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105412128-C-A

6630786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105412128-C-T

http://identifiers.org/hco/11/GRCh38#6630788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105412130-C-A

6630788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105412130-C-G

6630788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105412130-C-T

6630807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105412149-T-C

6630807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105412149-T-G

6630822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105412164-G-A

6630822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105412164-G-T

6630846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105412185-G-A

6630846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105412185-G-T

6630871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105412210-G-A

6630871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105412210-G-T

6630901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105412240-G-A

6630901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105412240-G-T

6630918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105412257-T-C

6630959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105412290-G-T

6630995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105412322-G-T

6631082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105412414-G-C

6631082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105412414-G-T

6631240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105412576-T-C

6631272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105412607-T-A

6631272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105412607-T-C

6631383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105412717-T-C

6631404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105412738-G-C

6631473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105412808-C-G

6631484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105412819-G-A

6631679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105413023-G-C

6631682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105413026-G-A

http://identifiers.org/hco/11/GRCh38#6631963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105413297-C-A

6631963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105413297-C-T

http://identifiers.org/hco/11/GRCh38#6631979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105413313-C-A

6631979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105413313-C-T

http://identifiers.org/hco/11/GRCh38#6631980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105413314-C-A

6631980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105413314-C-G

6631980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105413314-C-T

http://identifiers.org/hco/11/GRCh38#6632048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105413368-C-A

6632048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105413368-C-T

6632098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105413418-T-C

6632392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105413712-T-C

6632505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105413825-G-A

http://identifiers.org/hco/11/GRCh38#6632558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105413878-C-A

6632558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105413878-C-T

6632577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105413897-T-A

6632577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105413897-T-C

6632577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105413897-T-G

6632823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105414143-G-T

6632851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105414171-C-T

6632956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105414276-C-T

6632963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105414283-C-T

6632973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105414293-G-C

http://identifiers.org/hco/11/GRCh38#6633155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105414450-C-A

6633155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105414450-C-T

6633366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105414590-G-A

6633366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105414590-G-T

http://identifiers.org/hco/11/GRCh38#6633472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105414664-C-A

6633472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105414664-C-T

6633536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105414728-G-A

6633536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105414728-G-T

http://identifiers.org/hco/11/GRCh38#6633668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105414859-C-A

6633699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105414887-G-C

6633720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105414908-G-A

6633945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105415139-G-A

6633945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105415139-G-T

6634051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105415244-G-A

6634070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105415263-G-A

6634097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105415286-G-A

6634097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105415286-G-T

6634176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105415365-G-T

6634179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105415368-C-T

6634252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105415441-C-G

6634263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105415452-G-C

6634316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105415505-G-A

6634316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105415505-G-C

6634337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105415527-C-G

6634337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105415527-C-T

6634639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105415927-A-G

http://identifiers.org/hco/11/GRCh38#6634708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105415998-A-C

6635077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105416308-G-A

http://identifiers.org/hco/11/GRCh38#6635265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105416733-C-A

6635265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105416733-C-T

6635564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105417136-C-T

6635709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105417283-A-G

6635728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105417304-A-G

6635852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105417430-G-A

6635923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105417492-T-C

6636037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105417574-T-C

6636090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105417628-G-C

http://identifiers.org/hco/11/GRCh38#6636101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105417639-A-C

6636861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105417940-T-A

6637453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105418490-A-T

6637488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105418550-C-T

6637657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105418922-A-G

6637847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105419082-G-A

6637880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105419118-C-T

6637913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105419151-T-C

6638632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105419785-A-T

6639432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105420264-C-T

6639498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105420330-A-G

6639509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105420341-C-G

6639509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105420341-C-T

6639686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105420515-A-G

6639686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105420515-A-T

http://identifiers.org/hco/11/GRCh38#6639707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105420536-C-A

6639707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105420536-C-T

6639796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105420619-C-T

6639802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105420625-G-A

6639802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105420625-G-T

http://identifiers.org/hco/11/GRCh38#6640129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105420952-C-A

http://identifiers.org/hco/11/GRCh38#6640193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105421016-C-A

6640193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105421016-C-G

6640193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105421016-C-T

http://identifiers.org/hco/11/GRCh38#6640210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105421033-A-C

6640210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105421033-A-G

6640257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105421080-G-A

6640257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105421080-G-T

6640414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105421237-A-T

6640585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105421408-C-T

6640911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105421734-G-A

6640911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105421734-G-C

6640911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105421734-G-T

6640912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105421735-G-A

6640912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105421735-G-C

6640912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105421735-G-T

6640981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105421804-C-T

6641131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105421954-G-A

http://identifiers.org/hco/11/GRCh38#6641490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105422313-C-A

6641490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105422313-C-G

6641490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105422313-C-T

6641510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105422333-G-A

6641510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105422333-G-T

6641527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105422338-C-T

6641544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105422355-G-C

6641544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105422355-G-T

6641694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105422493-G-A

6641694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105422493-G-T

6641757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105422556-G-A

6641757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105422556-G-T

http://identifiers.org/hco/11/GRCh38#6641784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105422583-C-A

6641823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105422624-G-A

6641823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105422624-G-T

6641867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105422656-G-A

6642224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105422951-C-T

6642532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105423210-G-A

http://identifiers.org/hco/11/GRCh38#6642725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105423410-A-C

6642996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105423772-G-A

http://identifiers.org/hco/11/GRCh38#6643032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105423805-C-A

6643032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105423805-C-G

6643032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105423805-C-T

6643033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105423806-G-A

6643057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105423828-G-T

6643064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105423835-A-G

6643118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105423878-G-C

6643271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105424030-G-C

6643319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105424075-A-G

6643346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105424095-C-G

6643371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105424120-T-C

6643469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105424176-A-G

6643485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105424190-C-T

6643631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105424317-G-A

6643904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105424515-A-T

6643969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105424599-T-C

6644232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105424869-T-C

6644340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105425086-A-G

6644421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105425165-C-T

6644699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105425412-T-A

6644699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105425412-T-C

6645637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105426502-G-A

6645642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105426504-A-G

6646348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105427200-T-C

6646397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105427249-G-A

6646397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105427249-G-T

6646833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105427632-G-A

6646967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105427769-G-C

6647234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105428041-G-C

6647849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105428595-G-T

6647853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105428599-C-T

6647905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105428651-G-A

6648110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105428834-G-A

6648127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105428852-G-C

6648128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105428853-C-G

6648128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105428853-C-T

6648221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105428929-G-A

6648221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105428929-G-C

http://identifiers.org/hco/11/GRCh38#6648252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105428958-A-C

6649392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105430048-G-C

6649439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105430099-T-A

6649439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105430099-T-G

6649460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105430123-G-A

6649616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105430263-C-T

6649793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105430375-A-G

6649822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105430404-G-T

6649880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105430466-G-T

6649903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105430499-T-C

6650363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105431011-G-A

6650661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105431218-C-T

6650726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105431298-T-C

6650942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105431931-G-A

6650942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105431931-G-C

6651028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105432062-C-T

6651098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105432119-G-C

6651192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105432183-T-C

6651472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105432469-G-A

6651932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105432891-C-T

6651964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105432917-T-A

6651964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105432917-T-C

6652671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105433648-T-C

6652828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105433777-G-A

6652862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105433806-G-C

6653014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105433942-A-G

6653251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105434156-T-A

6653415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105434367-G-A

6653415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105434367-G-C

6653751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105434659-G-A

6653784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105434690-C-G

6653966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105435056-T-A

6653966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105435056-T-G

6654729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105435750-G-A

6654919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105435940-G-A

6654951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105435972-C-G

6654951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105435972-C-T

6654952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105435973-C-G

6655109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105436125-A-T

http://identifiers.org/hco/11/GRCh38#6655269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105436287-A-C

6655269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105436287-A-G

http://identifiers.org/hco/11/GRCh38#6655433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105436445-A-C

6655433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105436445-A-G

6655433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105436445-A-T

http://identifiers.org/hco/11/GRCh38#6655449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105436462-A-C

6655449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105436462-A-G

6655449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105436462-A-T

http://identifiers.org/hco/11/GRCh38#6655519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105436532-A-C

6655519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105436532-A-G

6655538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105436551-G-C

http://identifiers.org/hco/11/GRCh38#6655594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105436597-C-A

6655594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105436597-C-T

6655675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105436678-G-A

6655675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105436678-G-C

6655675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105436678-G-T

6655684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105436685-G-C

6655684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105436685-G-T

http://identifiers.org/hco/11/GRCh38#6655701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#105436702-C-A

6655701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105436702-C-G

6655701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13681
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105436702-C-T