54939442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: 47476476-T-C

54939705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: 47476708-C-G

54939705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: 47476708-C-T

54940048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: 47476958-G-T

54940422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: 47478025-C-T

http://identifiers.org/hco/14/GRCh38#54940454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47478056-C-A

54940454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: 47478056-C-G

http://identifiers.org/hco/14/GRCh38#54940594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47478174-C-A

54940697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: 47478270-T-A

http://identifiers.org/hco/14/GRCh38#54940733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47478303-C-A

54940733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: 47478303-C-T

http://identifiers.org/hco/14/GRCh38#54940875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47478385-C-A

54940959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: 47478467-T-C

54940966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: 47478474-T-C

54941093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: 47478594-G-T

http://identifiers.org/hco/14/GRCh38#54941166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47478670-C-A

54941166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3 prime UTR variant
orthologous variants: 47478670-C-T

54941220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47478725-A-G

54941230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47478735-G-A

54941230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47478735-G-T

54941260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47478762-G-A

54941260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47478762-G-T

http://identifiers.org/hco/14/GRCh38#54941279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47478771-C-A

54941279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47478771-C-T

54941281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47478773-T-A

54941281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47478773-T-G

54941285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47478777-G-A

54941285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47478777-G-T

54941297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47478790-T-A

54941344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47478831-A-T

54941392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47478906-T-C

54941430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47479008-G-C

54941430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47479008-G-T

54941480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47479060-C-T

54941481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47479061-T-A

54941493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47479072-C-T

54941511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47479090-A-G

54941517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47479096-T-A

54941517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47479096-T-C

54941539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47479118-T-C

54941604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47479183-T-C

54941642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47479221-C-T

54941741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47479321-T-A

54941741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47479321-T-C

54941753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47479335-G-A

54941753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47479335-G-T

54943089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47480386-C-T

54943091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47480388-T-C

54943099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47480395-G-A

54943209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47480476-T-A

54943451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47480612-G-A

http://identifiers.org/hco/14/GRCh38#54943474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47480626-A-C

54943490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47480638-G-A

54944101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47481031-T-G

54944182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47481101-G-A

54944182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47481101-G-T

54944222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47481131-T-C

54944230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47481139-T-A

54944231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47481140-T-C

54944248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47481168-A-G

54944289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47481218-T-G

54944510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47481434-C-T

54945244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47481843-T-C

54945244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47481843-T-G

54945400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482015-A-G

54945466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482080-G-C

54945524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482133-A-G

http://identifiers.org/hco/14/GRCh38#54955549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47482430-C-A

54955549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482430-C-T

54955551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482432-A-G

54955602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47482480-T-G

http://identifiers.org/hco/14/GRCh38#54957175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47482885-C-A

54957175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47482885-C-T

54957221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482930-T-C

54957221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482930-T-G

54957256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482964-T-A

http://identifiers.org/hco/14/GRCh38#54957266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47482977-C-A

54957266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482977-C-T

http://identifiers.org/hco/14/GRCh38#54957276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47482982-C-A

54957276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482982-C-T

54957278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482984-T-C

54957282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482988-A-G

54957283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47482989-T-C

http://identifiers.org/hco/14/GRCh38#54957307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47483013-C-A

54957307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47483013-C-T

54957318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47483024-A-T

54957337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47483046-A-G

http://identifiers.org/hco/14/GRCh38#54957447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47483163-C-A

54957533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47483244-A-G

54957669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47483361-G-A

54957669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47483361-G-T

54957671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47483363-A-G

54957673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47483380-A-G

54958008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47483789-T-C

http://identifiers.org/hco/14/GRCh38#54958564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47484005-C-A

http://identifiers.org/hco/14/GRCh38#54958585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47484025-C-A

54958585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47484025-C-G

54958694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47484125-T-G

54958848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47484260-C-T

54962569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47484908-G-T

54962585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47484923-G-A

54962585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47484923-G-C

54962585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47484923-G-T

54962593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47484931-T-C

54962593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47484931-T-G

http://identifiers.org/hco/14/GRCh38#54962694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47485025-C-A

54962850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47485352-G-A

54962850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 47485352-G-C

54962850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 47485352-G-T

54962978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47485479-T-A

54963189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47485679-G-A

54963189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47485679-G-C

54963189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47485679-G-T

http://identifiers.org/hco/14/GRCh38#54963251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47485756-A-C

54963285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47485789-C-T

54963402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47485908-G-T

54965312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47487591-C-T

54965631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47487864-C-T

54966353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47487943-A-G

54966373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47487963-T-A

54966373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47487963-T-C

http://identifiers.org/hco/14/GRCh38#54966395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47487985-C-A

http://identifiers.org/hco/14/GRCh38#54966472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47488214-C-A

54966505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47488247-C-T

54966628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47488369-C-T

54966755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47488701-G-T

54966777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47488723-T-C

http://identifiers.org/hco/14/GRCh38#54966797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47488744-C-A

54966797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47488744-C-G

54967074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47488984-A-G

54967080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47488990-T-C

http://identifiers.org/hco/14/GRCh38#54967156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47489170-C-A

54967156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47489170-C-T

54967192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47489294-A-T

54967247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47489347-A-G

54967251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47489351-C-T

54967438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47489534-T-C

54973410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47489733-T-A

54973664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47490171-G-C

54973852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47490332-G-A

54974128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47490542-A-G

54974343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47490807-G-A

http://identifiers.org/hco/14/GRCh38#54974414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47490867-C-A

54974414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47490867-C-G

54974414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47490867-C-T

54976074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47491054-C-G

54976074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47491054-C-T

54976126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47491097-T-G

54976192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47491162-C-G

54978188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47492683-A-T

54978282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47492760-C-T

54981523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47493544-T-C

http://identifiers.org/hco/14/GRCh38#54981704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47493725-C-A

54981710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47493734-G-A

54981710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47493734-G-T

54981731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47493752-G-A

54981731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47493752-G-C

54981731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47493752-G-T

http://identifiers.org/hco/14/GRCh38#54983807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47495058-C-A

54983935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47495109-G-T

54984033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47495225-A-G

54984179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47495360-T-A

http://identifiers.org/hco/14/GRCh38#54984787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47496042-C-A

54984787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47496042-C-T

54984806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47496061-T-C

54984879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47496131-T-A

54984879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47496131-T-C

54984913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47496164-C-T

54984938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47496189-T-C

54984948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47496199-G-A

54985666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47497426-G-A

54985685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47497431-G-A

54985762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47497502-G-C

54986553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47498206-T-A

54986655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47498309-G-T

54986662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47498316-T-A

54986729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47498373-A-G

54986759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47498393-G-T

54986975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47498594-C-T

http://identifiers.org/hco/14/GRCh38#54988708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47500652-C-A

54988708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500652-C-T

54988762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500692-T-A

54988917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500832-T-C

54988919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500834-T-A

http://identifiers.org/hco/14/GRCh38#54988933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47500848-A-C

54989036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 47500904-T-C

54989109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 47500977-G-T

54989245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501105-G-C

54989288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501148-A-T

54989301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501159-A-G

54989336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501277-G-A

54989336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501277-G-T

54989414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501464-T-G

54989458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501501-G-T

54989633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501676-A-G

54989736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501755-C-T

54989804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501791-T-G

54989986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501861-C-T

54990329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502129-G-A

54990393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502193-C-T

54991081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47503001-T-C

http://identifiers.org/hco/14/GRCh38#54991117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47503036-A-C

54991117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47503036-A-G

54991129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47503048-T-C

http://identifiers.org/hco/14/GRCh38#54991225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47503143-A-C

54991225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 47503143-A-G

http://identifiers.org/hco/14/GRCh38#54991350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47503268-C-A

54991532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47503455-T-A

54991533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47503456-G-T

http://identifiers.org/hco/14/GRCh38#54995452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47504316-C-A

54995452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47504316-C-T

54995513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47504366-T-C

http://identifiers.org/hco/14/GRCh38#54995553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47504385-C-A

54995553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47504385-C-G

54995669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 47504486-G-A

54995670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 47504487-G-A

54995670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 47504487-G-T

http://identifiers.org/hco/14/GRCh38#55000635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47505661-A-C

55000635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: synonymous variant
orthologous variants: 47505661-A-G

55000852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47506080-G-A

55000852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47506080-G-T

http://identifiers.org/hco/14/GRCh38#55001036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47506257-C-A

55001036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47506257-C-T

55001143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47506306-T-A

55001143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47506306-T-C

http://identifiers.org/hco/14/GRCh38#55001194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47506359-A-C

55001583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: -A-G

55006718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509308-A-G

55007089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509356-A-G

55007112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509379-C-T

55007121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509387-G-A

55007125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509391-G-A

55007131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509397-G-A

55007131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509397-G-C

55007170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509421-G-A

55007170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509421-G-T

55007171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509422-T-A

55007202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509457-T-A

55007202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509457-T-C

55007202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509457-T-G

http://identifiers.org/hco/14/GRCh38#55007209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47509464-C-A

55007209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509464-C-T

http://identifiers.org/hco/14/GRCh38#55007244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47509495-A-C

55007334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: synonymous variant
orthologous variants: 47509647-A-G

55007852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47509867-C-T

55007982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47510000-A-G

55008041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47510065-T-C

55008225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47510235-A-G

55008296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47510304-A-G

55008334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: synonymous variant
orthologous variants: 47510342-C-T

http://identifiers.org/hco/14/GRCh38#55008385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47510395-C-A

55008385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47510395-C-T

http://identifiers.org/hco/14/GRCh38#55008582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47510546-C-A

55010473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47511538-T-C

55010473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47511538-T-G

55010488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47511553-T-G

55010513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47511579-G-A

55010513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47511579-G-T

55010587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47511651-T-A

55010587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47511651-T-C

55010639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47511694-T-C

55010659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47511715-C-T

http://identifiers.org/hco/14/GRCh38#55011065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47512076-C-A

55011065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47512076-C-T

http://identifiers.org/hco/14/GRCh38#55013533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47512249-A-C

55013533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 47512249-A-G

55013559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 47512275-T-C

55014427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47512541-T-C

55014575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47512670-G-A

55014575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47512670-G-T

http://identifiers.org/hco/14/GRCh38#55014592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#47512687-C-A

55014696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47512799-T-C

55026512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47513790-G-T

55026575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: intron variant
orthologous variants: 47513851-A-G

55026855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47514100-C-T

http://identifiers.org/hco/14/GRCh38#55026923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#47514144-C-A

55026946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47514167-G-A

55026946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47514167-G-T

55026973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47514191-G-A

55027013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47514232-G-A

55027013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 47514232-G-T

http://identifiers.org/hco/14/GRCh38#55027029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#47514248-C-A

55027029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, splice_region_variant, undefined
orthologous variants: 47514248-C-G

55027029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23170
most severe consequence: 5_prime_UTR_variant, splice_region_variant, undefined
orthologous variants: 47514248-C-T