http://identifiers.org/hco/12/GRCh38#21437676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#142291401-C-A

21437676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 142291401-C-G

21437730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 142291458-C-T

21437867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142291591-G-A

21437867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142291591-G-C

21437867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142291591-G-T

http://identifiers.org/hco/12/GRCh38#21437884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#142291600-C-A

http://identifiers.org/hco/12/GRCh38#21437889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#142291605-C-A

21437889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142291605-C-T

http://identifiers.org/hco/12/GRCh38#21437894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#142291610-C-A

21437894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142291610-C-T

21437997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142291691-T-C

21437997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142291691-T-G

http://identifiers.org/hco/12/GRCh38#21438045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142291732-C-A

http://identifiers.org/hco/12/GRCh38#21438078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#142291761-A-C

21438492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142291855-T-C

21438835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142292097-G-A

21439305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142292485-C-T

21439793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142292777-A-G

21439981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142292951-A-G

21440118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142293060-C-T

21440153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142293084-T-A

21440153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142293084-T-C

21440193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142293126-C-T

21440205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142293138-A-G

21440205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142293138-A-T

21440249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142293191-G-A

21440249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142293191-G-T

21440461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142293377-G-A

21440461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142293377-G-C

21440461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142293377-G-T

21440526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142293441-T-A

21445278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142294182-T-A

21445393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 142294295-C-T

http://identifiers.org/hco/12/GRCh38#21445394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142294296-C-A

21445394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 142294296-C-T

21445454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 142294356-G-A

21445480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142294382-T-C

http://identifiers.org/hco/12/GRCh38#21445549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142294449-C-A

21445549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142294449-C-G

21445549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142294449-C-T

21445825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142294685-T-G

21448365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142295653-T-G

21448388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142295676-T-C

21448793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142296022-G-A

21448913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142296118-A-G

21449107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142296411-T-C

21449177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142296481-A-G

21449232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142296564-T-A

21449271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142296586-T-G

http://identifiers.org/hco/12/GRCh38#21449437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142296705-C-A

21449437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142296705-C-G

21449437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142296705-C-T

21449480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142296749-T-C

21449534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142296757-T-C

21449534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142296757-T-G

21449589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 142296814-G-T

21449610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 142296835-T-C

21449664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 142296889-A-T

21449761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142296977-A-G

21449796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142297013-A-G

21451374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142298580-C-T

21451464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142298708-G-A

21451530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142298774-A-G

21451621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142298858-G-A

21451694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142298913-A-G

21451750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142298965-G-A

21451750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142298965-G-T

21451967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299155-T-A

http://identifiers.org/hco/12/GRCh38#21451969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142299157-C-A

21451969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299157-C-T

21451989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299177-A-G

21452013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299199-A-G

http://identifiers.org/hco/12/GRCh38#21452038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142299211-C-A

21452038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299211-C-T

21452039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299212-A-G

21452134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 142299304-T-C

21452212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299339-T-A

21452212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299339-T-C

21452265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299388-G-C

21452265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299388-G-T

21452312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299427-C-G

21452326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299441-C-G

21452326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299441-C-T

21452638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142299652-T-A

21455112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 142300331-A-G

21455177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 142300396-A-G

21455260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 142300479-T-C

21455462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142301688-T-A

21455462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142301688-T-G

21455589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142301786-G-A

21455885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142302082-G-A

21455885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142302082-G-C

21455885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142302082-G-T

21455890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142302087-G-A

21455959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142302174-T-C

http://identifiers.org/hco/12/GRCh38#21456190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142302351-C-A

21456190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142302351-C-T

21456192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142302353-G-A

21456192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142302353-G-C

21456192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142302353-G-T

21456217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142302376-T-A

21456217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142302376-T-C

21456217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142302376-T-G

21456221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142302380-G-A

21456221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142302380-G-T

21456257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142302416-G-A

21460011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142302615-C-T

http://identifiers.org/hco/12/GRCh38#21461009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142303089-A-C

21461009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 142303089-A-G

http://identifiers.org/hco/12/GRCh38#21461072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142303153-C-A

21461095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 142303176-T-A

21461176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142303250-A-G

21461222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142303274-G-A

21461222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142303274-G-C

21461222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142303274-G-T

http://identifiers.org/hco/12/GRCh38#21461370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142303378-A-C

21461449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142303454-A-G

21461544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142303553-A-G

http://identifiers.org/hco/12/GRCh38#21461678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142303682-A-C

http://identifiers.org/hco/12/GRCh38#21461929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142304048-C-A

21461929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304048-C-T

21461930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304049-A-G

http://identifiers.org/hco/12/GRCh38#21461946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142304069-C-A

21461946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304069-C-T

21461947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304070-T-G

21461948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304071-G-A

21461948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304071-G-T

21461957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304078-A-G

21461957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304078-A-T

http://identifiers.org/hco/12/GRCh38#21461970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142304088-C-A

21461970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304088-C-G

21462010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 142304127-A-G

21462187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304300-T-C

21462216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304322-A-G

http://identifiers.org/hco/12/GRCh38#21462226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142304332-C-A

21462226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304332-C-G

http://identifiers.org/hco/12/GRCh38#21462273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142304360-A-C

21462273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304360-A-G

21462273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304360-A-T

21462327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304409-T-C

21462342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304420-A-G

21462388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304461-C-G

21462481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304535-C-G

21462481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304535-C-T

21462483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304537-T-G

21462572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304621-T-C

http://identifiers.org/hco/12/GRCh38#21462602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142304635-A-C

21462607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304640-T-C

21462607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304640-T-G

http://identifiers.org/hco/12/GRCh38#21462645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142304679-C-A

21462660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304694-T-A

21462694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304720-G-A

21462694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304720-G-T

21462718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304742-G-A

21462732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 142304754-T-C

21462732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 142304754-T-G

21462778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 142304800-T-A

21462778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 142304800-T-C

21462876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304898-T-A

21462876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304898-T-C

21462923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304938-T-G

http://identifiers.org/hco/12/GRCh38#21462928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142304943-C-A

21462928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304943-C-T

http://identifiers.org/hco/12/GRCh38#21462941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142304956-C-A

21462951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142304964-T-C

21463059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142305060-G-T

21467486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 142306590-G-A

21467553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 142306657-G-A

21467553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 142306657-G-C

21467553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 142306657-G-T

http://identifiers.org/hco/12/GRCh38#21467664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142306767-A-C

21467664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142306767-A-G

21467664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142306767-A-T

21467713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142306797-A-T

21468186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142307195-T-G

21468223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 142307225-C-T

http://identifiers.org/hco/12/GRCh38#21468451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142307416-C-A

http://identifiers.org/hco/12/GRCh38#21468601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142307575-C-A

21468601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 142307575-C-T

21468825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 142307792-A-G

21468825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 142307792-A-T

21468882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142307847-T-C

http://identifiers.org/hco/12/GRCh38#21468899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142307864-A-C

http://identifiers.org/hco/12/GRCh38#21468920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142307882-A-C

21468920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 142307882-A-G

http://identifiers.org/hco/12/GRCh38#21469906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142308226-C-A

21469906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3 prime UTR variant
orthologous variants: 142308226-C-G

21470069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3 prime UTR variant
orthologous variants: 142308329-G-A

21470292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 142308541-T-G

21470339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 142308588-G-A

21470339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 142308588-G-C

21470339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: 142308588-G-T

http://identifiers.org/hco/12/GRCh38#21470340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142308589-A-C

21470340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 142308589-A-T

21470492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 142308701-T-A

21470510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 142308720-T-C

21470513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 142308723-A-G

21470550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 142308781-T-A

21470550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 142308781-T-C

http://identifiers.org/hco/12/GRCh38#21470581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#142308816-C-A

21470582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 142308817-A-T

21470614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 142308854-G-C

21470873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 142309207-G-C

21470873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26162
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 142309207-G-T