63432342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 105824567-C-T

63432611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3 prime UTR variant
orthologous variants: 105824817-T-A

63432611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3 prime UTR variant
orthologous variants: 105824817-T-C

63432632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3 prime UTR variant
orthologous variants: 105824839-T-C

63432655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 105824862-A-G

63432696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3 prime UTR variant
orthologous variants: 105824903-G-A

63432742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3 prime UTR variant
orthologous variants: 105824931-G-A

63432742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3 prime UTR variant
orthologous variants: 105824931-G-T

63432749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3 prime UTR variant
orthologous variants: 105824938-G-A

http://identifiers.org/hco/17/GRCh38#63432799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105824981-C-A

63432799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3 prime UTR variant
orthologous variants: 105824981-C-T

63432839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3 prime UTR variant
orthologous variants: 105825009-A-T

http://identifiers.org/hco/17/GRCh38#63432984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105825097-A-C

63433322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 105825196-G-C

63433337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 105825214-T-C

63433383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 105825251-T-C

63433423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 105825296-G-T

63433433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105825306-A-G

63433488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105825367-G-A

63433488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105825367-G-C

63433488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105825367-G-T

63433536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105825426-T-C

63433633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105825508-G-A

63433818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105825662-A-G

63433842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105825680-A-G

63433843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105825681-G-T

http://identifiers.org/hco/17/GRCh38#63433850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105825688-A-C

63433850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105825688-A-G

63433850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105825688-A-T

63433957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105825778-G-A

63433980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105825801-C-T

http://identifiers.org/hco/17/GRCh38#63434000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105825825-C-A

http://identifiers.org/hco/17/GRCh38#63434034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105825860-C-A

63434034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105825860-C-T

63434080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105825888-T-C

63434080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105825888-T-G

http://identifiers.org/hco/17/GRCh38#63434164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105825961-C-A

63434164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105825961-C-T

63434172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105825969-G-C

63434172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105825969-G-T

63434206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105826017-T-A

63434206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105826017-T-G

63434207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105826018-G-A

63434207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105826018-G-T

63434332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105826128-A-G

63434552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105826351-G-A

63434552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105826351-G-C

63434552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105826351-G-T

63434561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105826360-G-A

63434614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105826412-G-A

63434854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105826503-G-A

63435014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105826535-G-A

63435055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105826553-G-T

63435079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105826571-C-T

http://identifiers.org/hco/17/GRCh38#63435185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105826677-C-A

63435185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105826677-C-T

63435232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 105826724-G-A

63435232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 105826724-G-C

63435232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 105826724-G-T

63435571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 105826902-C-T

http://identifiers.org/hco/17/GRCh38#63435598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105826931-C-A

63435598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105826931-C-T

63435609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105826940-G-A

63435609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105826940-G-T

63435857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105827179-A-G

63436035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105827362-G-A

63436039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105827366-C-T

http://identifiers.org/hco/17/GRCh38#63436041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105827368-C-A

63436064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 105827391-G-A

63436064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 105827391-G-T

63436155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 105827483-G-A

63436253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105827556-G-A

63436253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105827556-G-T

http://identifiers.org/hco/17/GRCh38#63436276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105827568-C-A

http://identifiers.org/hco/17/GRCh38#63436295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105827587-A-C

63436295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105827587-A-G

http://identifiers.org/hco/17/GRCh38#63436299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105827591-C-A

http://identifiers.org/hco/17/GRCh38#63436432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105827687-C-A

63436432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105827687-C-T

http://identifiers.org/hco/17/GRCh38#63436442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105827699-C-A

63436564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105827777-T-C

63436611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105827825-T-C

63436672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105827874-G-C

63436722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105827922-C-T

63436740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105827939-G-A

63436740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105827939-G-T

http://identifiers.org/hco/17/GRCh38#63436742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105827941-C-A

63436941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105828085-G-A

http://identifiers.org/hco/17/GRCh38#63436963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105828107-C-A

63436963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105828107-C-T

63437099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105828211-T-G

http://identifiers.org/hco/17/GRCh38#63437449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105828558-C-A

63437506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 105828615-A-G

63437535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105828641-C-T

63437563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105828669-G-A

http://identifiers.org/hco/17/GRCh38#63437968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105828746-C-A

63437968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105828746-C-G

63437968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105828746-C-T

63438079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105828860-G-A

63438079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105828860-G-C

63438146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105828911-A-G

63438204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105828972-T-C

63438208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105828976-C-G

63438208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105828976-C-T

http://identifiers.org/hco/17/GRCh38#63438239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105829008-C-A

63438239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105829008-C-T

http://identifiers.org/hco/17/GRCh38#63438330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105829073-C-A

63438330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829073-C-T

63438348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829091-G-A

63438348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829091-G-C

63438348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829091-G-T

63438443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829172-C-T

63438448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829179-C-T

63438494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829228-G-A

63438494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829228-G-C

63438638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829319-C-G

63439074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829734-G-A

63439074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829734-G-T

http://identifiers.org/hco/17/GRCh38#63439109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105829770-C-A

63439109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829770-C-T

63439147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105829814-G-T

http://identifiers.org/hco/17/GRCh38#63439184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105829851-C-A

63439184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105829851-C-T

63439210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105829866-A-G

http://identifiers.org/hco/17/GRCh38#63439230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105829879-C-A

63439753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830055-G-C

63440052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830298-T-A

63440066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830312-C-T

63440081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830327-A-G

63440158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830407-G-T

63440205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105830419-A-G

http://identifiers.org/hco/17/GRCh38#63440295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105830485-C-A

http://identifiers.org/hco/17/GRCh38#63440327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105830503-C-A

63440327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830503-C-T

63440419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830591-T-C

63440599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830735-G-A

63440599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830735-G-T

http://identifiers.org/hco/17/GRCh38#63440665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105830831-A-C

63440665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830831-A-G

63440665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830831-A-T

63440714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830913-G-A

63440714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105830913-G-T

63440811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105831040-T-G

63440962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105831183-G-C

63440962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105831183-G-T

http://identifiers.org/hco/17/GRCh38#63441008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105831200-A-C

63441066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105831268-C-T

63441140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105831346-G-A

63441233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105831439-G-A

63441238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105831444-C-T

63441251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105831456-T-A

63441251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105831456-T-C

63441350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105831554-G-A

63441735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832011-C-T

63441819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832079-C-T

63441879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832108-T-C

http://identifiers.org/hco/17/GRCh38#63441920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105832141-C-A

63441920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832141-C-G

63441920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832141-C-T

63441938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832151-G-A

63441938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832151-G-T

63441956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832169-A-G

63442194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832378-G-C

63442208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832394-A-G

63442227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832408-C-T

63442438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832527-C-T

63442647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832708-C-G

63442647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832708-C-T

63442648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832709-A-G

http://identifiers.org/hco/17/GRCh38#63442663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105832724-C-A

63442663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105832724-C-T

63442701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105832757-G-A

63442701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105832757-G-T

http://identifiers.org/hco/17/GRCh38#63442749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105832788-C-A

63442749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832788-C-G

63442749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832788-C-T

http://identifiers.org/hco/17/GRCh38#63442826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105832867-C-A

63442850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105832892-G-A

63442850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105832892-G-T

63442890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105832932-A-G

63442957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832993-G-A

63442957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105832993-G-T

63443181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105833173-A-G

63445405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834243-T-C

63445405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834243-T-G

63445418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834254-G-C

63445432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834268-C-T

63445438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834274-A-T

63445534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834347-G-C

63445595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834386-G-C

63445601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834401-A-G

63445601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834401-A-T

63445688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834477-G-A

63445773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834559-A-T

63445836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834617-T-C

63445837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105834618-C-T

63445855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105834626-A-G

63445887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105834658-T-G

63445901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105834671-G-T

63446023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105834774-G-A

63446023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105834774-G-T

http://identifiers.org/hco/17/GRCh38#63446033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105834788-C-A

http://identifiers.org/hco/17/GRCh38#63446036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105834792-C-A

63446045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105834801-G-A

63446045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105834801-G-T

63446125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105834849-G-A

63446125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105834849-G-C

63446125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105834849-G-T

http://identifiers.org/hco/17/GRCh38#63446189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105834881-C-A

63446189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105834881-C-T

63446218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105834913-G-A

63446218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105834913-G-T

63446235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105834927-G-C

63446235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105834927-G-T

63446241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105834933-C-T

63446247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 105834939-T-G

63446308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105835003-C-T

63446410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 105835063-G-A

63446424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 105835077-C-T

63446476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 105835120-G-A

63446476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 105835120-G-T

63446593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2571
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 105835190-G-A