23521000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55299259-C-T

23521203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55299468-G-A

23521203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55299468-G-C

23521312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55299566-A-G

23521360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55299612-T-C

23521429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55299675-G-A

23521625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55299834-A-G

23521739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55299883-G-A

23521739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55299883-G-T

23521775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55299914-T-C

23521775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55299914-T-G

http://identifiers.org/hco/14/GRCh38#23522236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55300335-C-A

23522236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55300335-C-G

23522236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55300335-C-T

23522321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55300420-G-A

23522454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55300553-C-T

23522685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55300784-T-A

23523013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301100-T-C

23523084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301166-T-A

23523084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301166-T-C

23523084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301166-T-G

23523085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301167-G-A

http://identifiers.org/hco/14/GRCh38#23523169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55301227-C-A

http://identifiers.org/hco/14/GRCh38#23523177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55301235-C-A

http://identifiers.org/hco/14/GRCh38#23523180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55301238-C-A

23523183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301241-C-T

23523330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55301392-T-G

23523363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55301425-T-C

23523653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55301715-C-G

23523653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55301715-C-T

http://identifiers.org/hco/14/GRCh38#23523654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55301716-C-A

23523654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55301716-C-T

http://identifiers.org/hco/14/GRCh38#23523855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55301917-A-C

23523855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55301917-A-G

23523975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55302034-G-A

23523978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55302037-G-A

23523979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55302038-G-A

23523979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55302038-G-T

23524167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55302226-A-G

23524189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55302248-C-T

23524401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55302460-C-T

23524494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55302553-G-A

23524494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55302553-G-T

http://identifiers.org/hco/14/GRCh38#23524521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55302580-C-A

23524521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55302580-C-T

23524560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55302625-T-C

23524616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55302681-T-C

23524701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55302763-T-C

http://identifiers.org/hco/14/GRCh38#23524859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55302918-C-A

23524859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55302918-C-T

23525173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55303232-A-G

23525230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55303289-G-A

23525350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55303409-G-A

23525350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55303409-G-C

23525404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55303463-C-T

23525949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55304008-G-A

23525949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55304008-G-T

23526027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55304086-G-A

23526027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55304086-G-T

23526040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55304099-T-C

23526071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55304130-T-A

23526071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55304130-T-C

23526087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55304146-A-G

23526099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55304158-A-G

23526100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55304159-G-C

23526100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55304159-G-T

23526180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55304239-T-C

23526225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55304284-G-A

23526225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55304284-G-T

http://identifiers.org/hco/14/GRCh38#23526236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55304295-C-A

23526450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55304509-T-C

23526629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55304688-G-C

23526636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55304695-A-G

23526774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55304878-C-G

23526774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55304878-C-T

23526935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55305030-C-G

23526935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55305030-C-T

http://identifiers.org/hco/14/GRCh38#23526998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55305095-C-A

23526998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305095-C-T

23527034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305130-T-C

http://identifiers.org/hco/14/GRCh38#23527050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55305146-C-A

23527050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305146-C-T

23527054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305150-T-A

23527054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305150-T-C

23527054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305150-T-G

23527115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305205-T-A

23527115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305205-T-C

23527167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305255-C-G

23527312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305383-C-G

23527332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305403-G-T

http://identifiers.org/hco/14/GRCh38#23527530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55305493-C-A

23527530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305493-C-T

23527616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55305577-C-T

23527727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55305688-T-A

23527849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305810-G-T

http://identifiers.org/hco/14/GRCh38#23527889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55305850-C-A

23527889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55305850-C-T

23528508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55306144-T-C

23528574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55306203-C-T

23528729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55306455-C-T

23528869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55306627-G-A

23529280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55306956-G-A

http://identifiers.org/hco/14/GRCh38#23529324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55307009-A-C

23529324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307009-A-G

http://identifiers.org/hco/14/GRCh38#23529354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55307022-C-A

http://identifiers.org/hco/14/GRCh38#23529374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55307048-C-A

23529374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307048-C-T

23529377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307051-T-C

23529395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307073-T-G

23529532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307192-G-A

23529532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307192-G-C

23529532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307192-G-T

23529546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307205-A-G

23529549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307208-G-A

23529549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307208-G-T

23529579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307238-A-G

23529691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55307577-C-T

http://identifiers.org/hco/14/GRCh38#23529839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55307736-A-C

23529839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307736-A-G

http://identifiers.org/hco/14/GRCh38#23529869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55307772-C-A

23529869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307772-C-T

23529879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307782-A-G

23529898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307801-G-T

23529974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307869-G-A

23529974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307869-G-T

23529987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55307882-T-C

23530016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55307900-T-C

http://identifiers.org/hco/14/GRCh38#23530122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55308020-A-C

23530130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55308028-T-C

http://identifiers.org/hco/14/GRCh38#23530266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55308222-A-C

23530266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55308222-A-T

23530315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55308267-G-A

23530315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55308267-G-C

23530315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55308267-G-T

23530384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55308329-A-G

23530429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55308354-T-G

23530457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308382-T-C

23530488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308405-C-T

23530515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308432-A-G

23530542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308457-G-A

23530542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308457-G-T

http://identifiers.org/hco/14/GRCh38#23530718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55308612-C-A

23530718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308612-C-T

23530719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308613-G-A

http://identifiers.org/hco/14/GRCh38#23530813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55308703-C-A

23530813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308703-C-T

23530842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308731-T-A

23530842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308731-T-C

23530923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308814-G-A

23530984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308908-G-A

23530984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308908-G-T

http://identifiers.org/hco/14/GRCh38#23530993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55308917-A-C

23531086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309005-A-G

23531252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309104-A-T

23531315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309163-G-T

23531333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309170-T-C

23531339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309176-T-A

http://identifiers.org/hco/14/GRCh38#23531374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55309208-C-A

23531374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309208-C-T

http://identifiers.org/hco/14/GRCh38#23531379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55309213-C-A

23531379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309213-C-T

http://identifiers.org/hco/14/GRCh38#23531444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55309281-C-A

23531444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309281-C-T

http://identifiers.org/hco/14/GRCh38#23531462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55309297-C-A

23531462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309297-C-T

23531495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309330-T-C

http://identifiers.org/hco/14/GRCh38#23531679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55309514-C-A

23531679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309514-C-T

http://identifiers.org/hco/14/GRCh38#23531680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55309515-C-A

23531680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55309515-C-T

http://identifiers.org/hco/14/GRCh38#23531780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55309615-A-C

23531780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309615-A-G

23531780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309615-A-T

23532145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309684-T-A

23532145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309684-T-C

23532145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309684-T-G

http://identifiers.org/hco/14/GRCh38#23532225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55309715-A-C

23532225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55309715-A-G

http://identifiers.org/hco/14/GRCh38#23532239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55309726-C-A

http://identifiers.org/hco/14/GRCh38#23532262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55309749-C-A

http://identifiers.org/hco/14/GRCh38#23532472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55309914-C-A

23532472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55309914-C-T

23532511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55309953-C-T

http://identifiers.org/hco/14/GRCh38#23532533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55309972-C-A

23532533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55309972-C-T

23532596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55310033-C-T

http://identifiers.org/hco/14/GRCh38#23532738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55310175-A-C

23532738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55310175-A-T

23532888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55310325-C-T

23533220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55310608-G-A

23533253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55310640-G-A

23533253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55310640-G-C

23533260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55310642-A-G

23533276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55310658-G-T

23533334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55310719-G-C

23533376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55310761-C-T

23533505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55310890-G-A

23533535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55310920-G-A

23533778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55311166-A-G

23534093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55311481-G-A

23534093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55311481-G-T

23534125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55311513-T-G

http://identifiers.org/hco/14/GRCh38#23534197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/14/GRCm39#55311585-C-A

23534292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55311686-G-A

23534354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55311748-G-A

23534354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55311748-G-T

23534387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55311781-G-A

23534412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55311800-G-C

23534587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 55311975-T-C

23534881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55312269-T-A

23534881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55312269-T-C

23534941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55312329-A-G

http://identifiers.org/hco/14/GRCh38#23535155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55312525-C-A

23535155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55312525-C-T

23535203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55312573-G-A

23535203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55312573-G-T

23535290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55312657-G-A

23535380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55312747-G-A

23537564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315066-A-T

23537594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315094-C-T

23537735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315172-C-G

23537735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315172-C-T

http://identifiers.org/hco/14/GRCh38#23537978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55315348-C-A

http://identifiers.org/hco/14/GRCh38#23538100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55315469-C-A

23538107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55315476-C-T

23538108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55315477-T-C

23538176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315541-T-C

23538334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315683-T-A

23538334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315683-T-C

23538438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315767-C-T

23538563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315892-C-G

23538593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315921-G-A

23538646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315971-G-A

http://identifiers.org/hco/14/GRCh38#23538772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55316078-A-C

23538902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55316167-G-A

http://identifiers.org/hco/14/GRCh38#23539327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55316571-C-A

23539388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55316607-G-A

23539429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55316646-T-C

http://identifiers.org/hco/14/GRCh38#23539636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55316810-C-A

23540765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55317162-A-G

http://identifiers.org/hco/14/GRCh38#23540816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55317216-C-A

23540840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55317239-C-T

23541751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55317677-C-T

23541867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55318539-C-G

http://identifiers.org/hco/14/GRCh38#23542055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55318705-C-A

23542055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55318705-C-T

23542067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55318717-G-A

23542067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55318717-G-T

23542100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55318748-A-G

23542100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55318748-A-T

http://identifiers.org/hco/14/GRCh38#23542193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55318806-C-A

23542193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55318806-C-T

23542195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55318808-T-C

http://identifiers.org/hco/14/GRCh38#23542250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55318861-C-A

23542370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55318961-A-G

23542382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55318973-G-A

23542382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55318973-G-C

23542382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55318973-G-T

23544550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55322792-C-T

23544618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55322853-G-A

http://identifiers.org/hco/14/GRCh38#23544944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55323158-A-C

23545046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55323248-C-G

23545046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55323248-C-T

23545633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55323889-A-G

23545633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55323889-A-T

23545887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324118-G-A

23546352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324565-T-C

23546437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324701-G-C

23546437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324701-G-T

23546510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55324835-G-A

23546654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55325046-C-T

23546828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55325221-C-T

23547012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55325384-G-A

http://identifiers.org/hco/14/GRCh38#23547262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55325598-C-A

23547273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55325609-G-A

23547549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55325856-A-G

23547573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55325866-A-G

23547730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55326002-G-C

23547733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55326005-G-A

23547783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55326037-T-C

http://identifiers.org/hco/14/GRCh38#23548260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55326648-C-A

23548260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55326648-C-T

23548412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55326796-A-G

23549021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55327348-A-G

23549652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55327891-G-A

23549652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55327891-G-C

23549702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55327941-C-T

23549743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55327975-T-C

23549985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55328223-G-A

23550006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55328244-G-A

23550910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55329012-G-T

23550996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55329098-C-T

http://identifiers.org/hco/14/GRCh38#23551201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55329278-C-A

23551201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55329278-C-T

23551228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55329306-G-A

23551228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55329306-G-T

23551712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55329806-T-A

23551712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55329806-T-C

23551858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55329952-C-T

23551902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55330044-C-G

23551979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55330128-T-C

23552204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55330440-A-G

http://identifiers.org/hco/14/GRCh38#23555581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55331805-C-A

23555581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55331805-C-G

23555778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55332040-A-G

23555803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55332071-G-C

23555803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55332071-G-T

http://identifiers.org/hco/14/GRCh38#23555861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55332104-C-A

http://identifiers.org/hco/14/GRCh38#23555905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55332142-C-A

23555909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55332146-G-A

23555909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55332146-G-T

23555926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55332166-T-A

23555964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55332197-G-A

23555964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55332197-G-T

23555968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55332201-C-T

23556048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55332280-C-T

23556121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55332348-G-A

23556121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20152
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55332348-G-T