http://identifiers.org/hco/3/GRCh38#11556148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114836954-C-A

11556148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114836954-C-T

http://identifiers.org/hco/3/GRCh38#11556151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114836957-C-A

11556151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114836957-C-T

11556274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114837075-A-T

11556478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114837256-G-T

11556871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114837655-G-A

11556871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114837655-G-T

http://identifiers.org/hco/3/GRCh38#11556936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114837712-A-C

11556936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114837712-A-G

11556969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114837742-A-G

11556990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114837763-A-G

11557700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114838351-T-C

11557762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114838416-T-C

11558009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114838604-G-T

11558167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114838749-G-A

11558167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114838749-G-T

11558203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114838779-G-C

11558203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114838779-G-T

11558300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114838870-G-A

11558314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114838884-G-C

11558314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114838884-G-T

http://identifiers.org/hco/3/GRCh38#11558472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114839030-A-C

11558472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114839030-A-G

11558472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114839030-A-T

11558643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114839213-G-A

11558685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114839255-C-T

11558739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114839309-G-A

11558739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114839309-G-T

11558820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114839390-G-A

11559161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114839571-A-T

http://identifiers.org/hco/3/GRCh38#11559196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114839601-C-A

11559196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114839601-C-G

11559196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114839601-C-T

http://identifiers.org/hco/3/GRCh38#11559255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114839660-C-A

11559255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114839660-C-T

11559414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114839799-G-A

11559414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114839799-G-T

11559420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114839805-G-A

11559420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114839805-G-T

11559497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114839906-G-A

11559497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114839906-G-C

11559497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114839906-G-T

http://identifiers.org/hco/3/GRCh38#11559508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114839917-C-A

11559508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114839917-C-T

11564727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114840773-G-A

11564727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114840773-G-C

11564727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114840773-G-T

11564746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114840794-A-G

http://identifiers.org/hco/3/GRCh38#11564863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114840887-C-A

11564863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114840887-C-G

11565033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114841054-A-G

11565068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114841083-G-A

11565068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114841083-G-T

http://identifiers.org/hco/3/GRCh38#11565126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114841146-C-A

11565126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114841146-C-T

11565143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114841151-G-A

11565143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114841151-G-T

11565174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114841163-G-A

11565183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114841172-G-A

11565196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114841184-T-C

11566367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114842314-C-T

11566417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114842334-G-C

11566422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114842339-C-T

11567005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114842729-G-A

http://identifiers.org/hco/3/GRCh38#11568668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#114843216-C-A

11568668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114843216-C-T

http://identifiers.org/hco/3/GRCh38#11568706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#114843241-C-A

11568706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114843241-C-T

11568707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114843242-G-A

11568707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114843242-G-T

http://identifiers.org/hco/3/GRCh38#11568805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114843321-C-A

11568805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114843321-C-T

http://identifiers.org/hco/3/GRCh38#11568853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#114843349-C-A

11568853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114843349-C-G

11568853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114843349-C-T

http://identifiers.org/hco/3/GRCh38#11568858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#114843354-C-A

11568883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114843372-C-T

11568918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114843390-G-A

11568918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114843390-G-C

11568961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114843415-G-A

11568974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843428-A-G

11569107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843564-G-A

11576356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114847023-C-T

11576450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114847121-C-T

11576598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114847265-G-A

11576863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114847460-A-G

11577129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114847666-G-C

11577146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114847680-G-A

11577165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114847699-G-C

11577189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114847719-T-G

http://identifiers.org/hco/3/GRCh38#11577228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114847754-A-C

11577261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114847791-G-C

11580315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114850638-G-A

11580316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114850639-G-A

11580499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114850824-G-A

11580620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114850950-T-C

http://identifiers.org/hco/3/GRCh38#11582418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114852116-C-A

http://identifiers.org/hco/3/GRCh38#11582454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114852147-C-A

11582454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114852147-C-T

http://identifiers.org/hco/3/GRCh38#11582462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114852155-C-A

11582462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114852155-C-G

11582462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114852155-C-T

11582947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114852506-G-A

11583002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114852540-G-A

11583110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114852617-A-G

11583119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114852625-G-A

11583430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114852891-G-T

11583834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114853193-A-G

11583873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114853219-C-T

11583919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114853259-C-T

11583999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114853331-G-A

11585731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114854764-G-A

11585878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114854916-T-A

11585878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114854916-T-C

11589423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114858656-G-A

11589579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114858790-T-G

11589715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114858845-G-A

11589811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114858918-C-G

11589940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114859030-G-A

11590176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114859190-C-T

11590451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114859449-A-G

11590469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114859467-G-C

11590565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114859525-C-T

11590838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114859705-C-T

11591269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114860084-C-T

11591493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114860301-C-G

http://identifiers.org/hco/3/GRCh38#11598888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114864651-C-A

11598888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114864651-C-G

11598902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114864665-C-G

11599474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114865232-C-T

http://identifiers.org/hco/3/GRCh38#11599972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114865515-A-C

11600008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114865549-G-A

11600371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114865835-A-T

11600384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114865848-G-A

11600421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114865886-G-A

11600670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114866131-A-G

http://identifiers.org/hco/3/GRCh38#11601979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#114867724-C-A

11601979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 114867724-C-G

11601979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 114867724-C-T

http://identifiers.org/hco/3/GRCh38#11602103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114867869-C-A

11602103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114867869-C-T

11602265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114868025-T-C

11602781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114868494-A-G

11602900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114868614-A-G

11603024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114868731-G-A

11603058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114868765-C-T

11603157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114868866-T-C

11603159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114868868-T-C

11603396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114869103-G-A

11603693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114869376-C-T

11610116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114870991-A-G

11610198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114871079-A-G

11610285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114871158-C-T

11610309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114871182-A-G

http://identifiers.org/hco/3/GRCh38#11610330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114871203-A-C

11610562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114871459-G-C

11610562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114871459-G-T

11618752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114878222-G-A

11618760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114878227-A-T

11618949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114878421-T-C

11619299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114878748-T-C

11619582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114879050-G-A

11619693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114879137-G-T

11620043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114879398-G-A

11620128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114879479-A-G

11622202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114880206-A-G

11622245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114880242-C-T

11622974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114880866-C-T

11623105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114880974-C-T

11623106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114880975-A-G

11626282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114882066-A-G

http://identifiers.org/hco/3/GRCh38#11626387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#114882194-C-A

11626405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114882215-T-C

11632387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114886072-A-G

11632527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114886200-C-T

11632564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114886239-C-T

11636293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114890291-A-G

11636439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114890459-A-G

11636574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114891112-C-G

11636629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114891164-T-C

11636814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114891353-T-G

11637839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114893085-C-T

11638138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114893385-T-C

11638357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114893789-G-A

11638357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114893789-G-C

http://identifiers.org/hco/3/GRCh38#11638367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114893799-C-A

11638385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114893818-A-G

11638516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114893937-T-A

11638517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114893938-T-C

11638563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114893993-G-A

11638564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114893994-G-A

11638568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114893998-C-T

11638642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114894091-C-G

11638735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114894186-T-G

http://identifiers.org/hco/3/GRCh38#11638807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114894247-A-C

http://identifiers.org/hco/3/GRCh38#11639005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114894465-A-C

11639016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114894476-G-A

11639016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114894476-G-T

11639182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114894650-G-C

http://identifiers.org/hco/3/GRCh38#11639264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114894719-C-A

11639264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114894719-C-T

11639280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114894739-G-A

11639492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114894926-G-A

11639953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114895058-A-G

11640050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114895135-C-G

11640243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114895307-G-C

11640333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114895412-G-A

11640480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114895567-G-A

11641105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114896047-G-A

11641105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114896047-G-T

11641111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114896053-T-A

11641111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114896053-T-C

http://identifiers.org/hco/3/GRCh38#11641275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114896105-C-A

11641451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114896455-C-T

http://identifiers.org/hco/3/GRCh38#11641539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114896544-C-A

11641539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114896544-C-T

11641720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114896724-A-G

11641754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114896757-C-T

11641903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114896883-A-G

11642023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114897015-A-T

11642214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114897164-G-C

11642464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114897353-T-C

11642467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114897356-A-G

11642476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114897365-G-A

11642484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114897376-G-A

11642712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114897553-A-G

11643281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114898129-A-T

11643372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114898218-C-T

11643396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114898242-G-A

11643396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114898242-G-C

11643396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114898242-G-T

11643565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114898410-G-T

11643642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114898489-G-A

11643642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114898489-G-T

11643659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114898506-A-T

11643669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114898520-T-A

11643670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114898521-A-T

11643683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114898540-T-A

11643683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114898540-T-C

http://identifiers.org/hco/3/GRCh38#11643694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114898551-A-C

11643786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114898638-G-A

11643786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114898638-G-C

http://identifiers.org/hco/3/GRCh38#11643795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114898647-A-C

http://identifiers.org/hco/3/GRCh38#11643882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114898735-C-A

11643882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114898735-C-G

11643882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114898735-C-T

http://identifiers.org/hco/3/GRCh38#11643930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114898783-C-A

11643930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114898783-C-T

11644028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114898870-G-A

11644037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114898878-G-T

11644271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114899122-T-C

11644281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114899132-T-C

11650277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114901805-A-T

11650337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114901868-A-G

11650622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114902083-C-G

11650622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114902083-C-T

11650833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114902249-G-T

11650914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114902322-T-C

11650930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114902338-G-C

11651151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114902475-T-A

http://identifiers.org/hco/3/GRCh38#11651201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114902514-A-C

11651201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114902514-A-T

11651283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114902585-T-C

11651332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114902632-G-A

11651477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114902772-C-G

11651524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114902811-G-C

11652215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114903598-T-C

11652351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114903765-T-C

11654864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114904711-T-C

11654888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114904735-C-T

11655357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114905567-T-C

11655394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114905604-G-A

11655749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114905825-C-G

11655749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114905825-C-T

11655769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114905843-G-A

11656022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114906074-G-A

11656025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114906077-C-T

11656104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114906161-T-C

11656217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114906297-G-A

http://identifiers.org/hco/3/GRCh38#11656218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114906298-A-C

11656225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114906305-T-C

11656652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114906561-G-A

11656706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114906631-T-C

11658386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114908344-C-T

11658534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114908491-C-G

11658651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114908620-T-C

11658703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114908674-A-G

11658748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114908731-G-T

11658825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114908789-G-C

11659145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114909111-A-T

11659273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114909214-A-G

11659732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114909315-C-T

11665080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114913628-G-A

11665080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114913628-G-T

11666523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114914297-A-T

11666557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114914331-G-T

11666632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114914405-A-G

11666747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114914547-G-A

11667045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114914888-C-T

11667262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114915094-T-C

11667413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114915199-G-A

http://identifiers.org/hco/3/GRCh38#11667447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114915232-A-C

11667511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114915277-T-C

11667546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114915312-C-T

11667564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114915330-C-T

11667878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114915716-G-T

http://identifiers.org/hco/3/GRCh38#11668143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: -C-A

11668143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: -C-T

11671107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114918019-C-T

11671115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114918027-A-G

11671115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114918027-A-T

11671126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114918038-A-G

11671314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 114918212-T-C

11671343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114918241-G-A

11671343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114918241-G-T

11671672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114918315-T-C

11671731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114918385-T-A

11671750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114918412-A-T

11675541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114921824-T-C

11675609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114921931-T-C

http://identifiers.org/hco/3/GRCh38#11675945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114922377-A-C

11676445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114923115-T-G

11690688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114926904-A-G

11690751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114926971-G-T

11690971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114927191-T-G

11690974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114927194-C-T

11692101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114929265-T-C

11692101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114929265-T-G

http://identifiers.org/hco/3/GRCh38#11692742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114929967-A-C

11692742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114929967-A-G

11692742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114929967-A-T

11692747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114929972-G-A

11698555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114932200-T-C

11698719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114932365-T-A

11698960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114932592-T-C

http://identifiers.org/hco/3/GRCh38#11699161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#114932792-C-A

11699161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114932792-C-T

http://identifiers.org/hco/3/GRCh38#11699435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114933162-C-A

11702811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934772-T-A

11702811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934772-T-C

11702818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934779-G-A

11702818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934779-G-C

11702818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934779-G-T

11702826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934787-G-T

http://identifiers.org/hco/3/GRCh38#11702860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114934822-A-C

11702860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934822-A-T

11702909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934869-G-A

11702909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934869-G-T

11703022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114934948-A-G

11703113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114935046-A-G

11703127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114935178-T-A

11703127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114935178-T-C

http://identifiers.org/hco/3/GRCh38#11703138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114935197-C-A

11703144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114935203-G-A

11703144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114935203-G-T

11703195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114935249-G-T

11703454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114935559-C-T

11703508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114935650-T-C

11703709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114935927-C-T

11703811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114936039-C-T

11710355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114938435-G-A

11710355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114938435-G-T

11710411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114938484-G-A

11710560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114938611-G-T

11710647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114938688-T-C

11710784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114938802-G-A

11711946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114939008-T-G

11713337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114940220-T-G

11713906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114940827-G-A

11714143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941114-A-G

11714236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941263-G-A

11715287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941533-C-G

11715383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941631-G-C

11715919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114942042-G-A

11716013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114942130-A-G

11716539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114942331-T-C

11716670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114942456-C-T

11718149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114944408-G-C

11718352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114944729-G-A

11718355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114944732-T-C

http://identifiers.org/hco/3/GRCh38#11719060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114945557-C-A

http://identifiers.org/hco/3/GRCh38#11719307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114945757-C-A

11719307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945757-C-T

http://identifiers.org/hco/3/GRCh38#11719371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114945787-C-A

11719371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945787-C-T

http://identifiers.org/hco/3/GRCh38#11719379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114945795-C-A

11719626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114945960-G-A

11719626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114945960-G-T

http://identifiers.org/hco/3/GRCh38#11719665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114945998-C-A

11719665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945998-C-G

11719665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945998-C-T

11719772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114946107-G-T

11719836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114946169-G-A

11720235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114946516-C-G

11720235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114946516-C-T

http://identifiers.org/hco/3/GRCh38#11720315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#114946580-C-A

11720315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114946580-C-T

11720316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114946581-C-T

11720335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114946600-G-A

11720335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114946600-G-T

11720463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114946750-G-A

11720463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114946750-G-T

11720481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114946768-G-A

11720481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114946768-G-T

11720483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114946770-C-T

11720548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114946811-A-T

http://identifiers.org/hco/3/GRCh38#11720676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114946899-C-A

11720676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114946899-C-T

http://identifiers.org/hco/3/GRCh38#11721094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114947276-C-A

http://identifiers.org/hco/3/GRCh38#11722168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114948934-C-A

11722168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114948934-C-T

http://identifiers.org/hco/3/GRCh38#11722243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114949007-A-C

11722462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949208-A-G

11722714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949408-T-C

11722770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949466-T-A

http://identifiers.org/hco/3/GRCh38#11738177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114952124-C-A

11738177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114952124-C-T

11738178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114952126-C-T

11738273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114952221-T-C

http://identifiers.org/hco/3/GRCh38#11738312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114952276-A-C

11738312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114952276-A-G

11739698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114953701-G-A

11739698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114953701-G-T

11739752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114953765-T-C

11740055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114954073-C-T

http://identifiers.org/hco/3/GRCh38#11740082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114954100-C-A

http://identifiers.org/hco/3/GRCh38#11740092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114954110-C-A

11749771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114957766-G-A

http://identifiers.org/hco/3/GRCh38#11749808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#114957793-A-C

11753693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114958218-C-G

11753693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114958218-C-T

11753720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114958239-G-A

11755587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114960076-G-A

11755593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114960082-G-T

11757647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114961431-G-C

11757654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114961438-T-C

11757702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114961537-G-A

11764990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114962612-A-G

11765023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114962640-T-C

11765288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114962893-C-T

11765506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114963103-G-A

11768457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114964052-G-C

11768506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114964088-T-A

11770423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114964867-G-A

11770461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron variant
orthologous variants: 114964903-A-G

11770743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114965231-T-C

11770791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114965269-C-T

11770861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114965347-G-C

11771004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114965477-G-A

11771004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: intron_variant, undefined
orthologous variants: 114965477-G-T

11771329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28966
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 114965827-G-T