50190563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44333205-G-A

50190675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44333117-C-T

50190701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44333092-C-G

50190701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44333092-C-T

50190794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44332995-C-G

50190852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44332941-G-T

50190918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44332860-C-G

50199286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44322653-G-A

50199565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44322407-G-A

50199623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44322321-T-C

50199671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44322275-G-A

50203535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44320360-G-A

50203535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44320360-G-C

50203535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44320360-G-T

50203809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44320097-T-A

50203809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44320097-T-C

http://identifiers.org/hco/19/GRCh38#50204072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44319832-C-A

http://identifiers.org/hco/19/GRCh38#50205402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44318814-C-A

50205402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44318814-C-T

http://identifiers.org/hco/19/GRCh38#50205523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44318690-C-A

50205535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 44318679-G-A

50205535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 44318679-G-T

50205630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44318463-C-T

http://identifiers.org/hco/19/GRCh38#50205643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44318450-C-A

50205643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44318450-C-T

50205664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44318428-C-T

50205670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44318423-T-A

50205670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44318423-T-C

50205708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44318353-T-G

50205774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44318259-G-A

50205774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44318259-G-T

50205830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44318174-C-T

50206508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44317514-C-T

http://identifiers.org/hco/19/GRCh38#50206558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44317485-A-C

50206748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44317338-C-G

50209989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44315159-T-C

50210067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44315128-C-T

50210118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44315074-A-G

50210123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44315069-A-G

50210123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44315069-A-T

http://identifiers.org/hco/19/GRCh38#50210403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44314882-C-A

50210403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 44314882-C-G

50210403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 44314882-C-T

http://identifiers.org/hco/19/GRCh38#50210420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44314865-C-A

50210420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 44314865-C-T

50210435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 44314850-G-A

50210471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 44314814-G-A

50210543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 44314754-T-C

50210612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 44314685-G-A

50210612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 44314685-G-T

50210823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44314504-G-T

50210860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44314469-G-C

50211965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44313686-G-C

http://identifiers.org/hco/19/GRCh38#50212009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44313643-A-C

50214226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44312774-C-T

50214307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44312691-A-G

50215000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 44312133-T-A

50217488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44310613-T-G

50217490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44310611-A-T

50217503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44310598-A-G

50217717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 44310384-G-A

http://identifiers.org/hco/19/GRCh38#50217816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44310300-C-A

50217816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44310300-C-G

50217816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44310300-C-T

50222775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307942-C-G

50222775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307942-C-T

50222851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307872-C-T

50222952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307777-A-T

50222953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307776-C-T

http://identifiers.org/hco/19/GRCh38#50222955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44307774-C-A

50222955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307774-C-T

50222977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307752-T-C

50223039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307706-G-C

50223202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307542-T-A

50223202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307542-T-C

http://identifiers.org/hco/19/GRCh38#50223213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44307493-C-A

50223213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307493-C-G

50223213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307493-C-T

50223223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307483-T-C

50223227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307479-T-A

50223229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307477-C-G

http://identifiers.org/hco/19/GRCh38#50223241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44307465-C-A

50223241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 44307465-C-G

50223241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 44307465-C-T

50223245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, splice_acceptor_variant
orthologous variants: 44307461-A-G

http://identifiers.org/hco/19/GRCh38#50223358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44307348-C-A

http://identifiers.org/hco/19/GRCh38#50223389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44307318-C-A

50223389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307318-C-T

http://identifiers.org/hco/19/GRCh38#50223399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44307310-C-A

http://identifiers.org/hco/19/GRCh38#50223468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44307249-C-A

50223468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307249-C-T

http://identifiers.org/hco/19/GRCh38#50223472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44307245-C-A

50223472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44307245-C-T

50224017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44306984-T-A

50224017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44306984-T-C

http://identifiers.org/hco/19/GRCh38#50224067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44306949-A-C

50224067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44306949-A-T

http://identifiers.org/hco/19/GRCh38#50224262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44306753-C-A

50224319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44306708-A-G

50224324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44306703-G-A

50224324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44306703-G-C

50224489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44305822-C-T

50224777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44305546-C-T

http://identifiers.org/hco/19/GRCh38#50225457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44305211-A-C

http://identifiers.org/hco/19/GRCh38#50225515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44305172-C-A

50225515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44305172-C-T

http://identifiers.org/hco/19/GRCh38#50225544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44305150-C-A

http://identifiers.org/hco/19/GRCh38#50225548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44305146-C-A

50225757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44304950-G-A

50225757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44304950-G-T

50225776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44304949-G-A

50226718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44304828-C-T

http://identifiers.org/hco/19/GRCh38#50226752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44304795-C-A

50226809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44304744-C-T

50226845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44304739-A-G

http://identifiers.org/hco/19/GRCh38#50230527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44303474-C-A

50230527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 44303474-C-T

50230545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 44303456-G-A

50230545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 44303456-G-T

50230624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, splice_donor_variant, undefined
orthologous variants: 44303377-G-C

50230624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, splice_donor_variant, undefined
orthologous variants: 44303377-G-T

50230638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44303363-G-A

50230638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44303363-G-T

50230642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 44303359-T-C

50232004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 44301919-C-T

http://identifiers.org/hco/19/GRCh38#50232010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44301913-C-A

50232010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 44301913-C-G

50232010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 44301913-C-T

50232058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 44301865-G-A

50232058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 44301865-G-T

50234386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44300253-G-T

http://identifiers.org/hco/19/GRCh38#50234394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44300249-C-A

50234598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44300117-G-A

50234598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44300117-G-C

50237651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44299663-G-C

http://identifiers.org/hco/19/GRCh38#50238030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44299336-A-C

50238152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44299217-A-G

50238185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44299175-C-T

50238203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44299160-G-A

50238207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44299156-T-C

http://identifiers.org/hco/19/GRCh38#50244221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44293001-C-A

50244221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44293001-C-T

http://identifiers.org/hco/19/GRCh38#50244268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44292955-C-A

50245479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44291762-G-A

http://identifiers.org/hco/19/GRCh38#50245485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44291756-C-A

50245727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44291535-A-G

http://identifiers.org/hco/19/GRCh38#50246877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44290694-C-A

50246877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44290694-C-T

50246913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44290660-C-T

http://identifiers.org/hco/19/GRCh38#50246916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44290657-A-C

50246916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44290657-A-G

50246933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44290642-A-G

50247132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44290473-G-A

50248298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44289315-C-T

50248351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44289264-G-C

50248693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44289032-C-T

50248700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44289026-C-T

50248836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44288932-T-C

50248890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 44288880-A-T

http://identifiers.org/hco/19/GRCh38#50248908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44288857-C-A

http://identifiers.org/hco/19/GRCh38#50249590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44288595-C-A

http://identifiers.org/hco/19/GRCh38#50249608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44288580-C-A

50249608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44288580-C-T

http://identifiers.org/hco/19/GRCh38#50249639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44288549-C-A

50249639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44288549-C-T

50249674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44288514-A-G

50249704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44288484-C-T

50249755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44288433-G-A

http://identifiers.org/hco/19/GRCh38#50249812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44288376-A-C

50249855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44288326-A-G

50249857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44288324-G-A

50249857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44288324-G-C

50249870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44288309-C-G

50249870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44288309-C-T

50250499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287895-T-G

50250596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44287804-G-A

http://identifiers.org/hco/19/GRCh38#50250623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44287777-A-C

50250710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287691-G-A

50250710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287691-G-T

50252361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287534-A-G

50252362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287533-C-T

50252368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287527-G-A

50252372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287523-G-A

50252515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287370-G-A

http://identifiers.org/hco/19/GRCh38#50252609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44287329-C-A

50252613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287326-G-A

50252613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287326-G-T

http://identifiers.org/hco/19/GRCh38#50252616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44287323-C-A

50252616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287323-C-T

50252617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287322-T-C

http://identifiers.org/hco/19/GRCh38#50252762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44287178-C-A

http://identifiers.org/hco/19/GRCh38#50252763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44287177-C-A

50252763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44287177-C-G

http://identifiers.org/hco/19/GRCh38#50255149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44285053-C-A

50255149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44285053-C-T

http://identifiers.org/hco/19/GRCh38#50255198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44285017-C-A

50255374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44284844-G-A

50255374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44284844-G-T

50255395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44284824-T-G

50255396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44284823-G-T

http://identifiers.org/hco/19/GRCh38#50255411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44284809-C-A

50255543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44284625-G-C

50257150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44284194-T-C

50257185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44284162-C-T

http://identifiers.org/hco/19/GRCh38#50257213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44284136-A-C

http://identifiers.org/hco/19/GRCh38#50257241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44284105-A-C

50257241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44284105-A-G

http://identifiers.org/hco/19/GRCh38#50257284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44283988-A-C

50257293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44283974-T-C

http://identifiers.org/hco/19/GRCh38#50257346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44283921-C-A

50257427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44283840-A-G

50257605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44283743-A-G

50257606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44283742-G-A

50259121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, undefined
orthologous variants: 44283033-G-A

50259121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, undefined
orthologous variants: 44283033-G-T

http://identifiers.org/hco/19/GRCh38#50259127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#44283027-C-A

50259127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, undefined
orthologous variants: 44283027-C-T

50259156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: stop gained
orthologous variants: 44283006-G-T

50259163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44282999-G-A

50259216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, undefined
orthologous variants: 44282946-T-C

50266970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44280174-G-A

50266970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44280174-G-T

50267039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, undefined
orthologous variants: 44280082-T-C

50267039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, undefined
orthologous variants: 44280082-T-G

50267040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, undefined
orthologous variants: 44280081-G-T

50267050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44280071-T-G

50267078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44280047-G-A

50267078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44280047-G-C

50267078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44280047-G-T

50267095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44280030-T-C

50267140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44279983-G-A

50267140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44279983-G-T

50268206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44279440-G-A

50268206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44279440-G-T

50268391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44279271-A-G

50268391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44279271-A-T

http://identifiers.org/hco/19/GRCh38#50271266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44278885-C-A

50271266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278885-C-T

50271284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278876-G-T

http://identifiers.org/hco/19/GRCh38#50271292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44278868-C-A

50271292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278868-C-G

50271292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278868-C-T

http://identifiers.org/hco/19/GRCh38#50271386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44278837-C-A

50271386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278837-C-T

http://identifiers.org/hco/19/GRCh38#50271392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44278831-C-A

50271393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278830-T-A

50271430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44278798-G-A

50271430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44278798-G-T

50271499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44278729-G-C

50271554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44278674-G-A

50271564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278648-A-T

http://identifiers.org/hco/19/GRCh38#50271573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44278639-A-C

50271573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278639-A-T

50271581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278548-T-G

50271583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278546-G-A

50271583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278546-G-T

50271585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278544-G-A

50271585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278544-G-T

50271587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278542-G-A

50271587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278542-G-T

50271589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278540-A-G

50271592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278537-G-A

50271592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278537-G-C

50271592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278537-G-T

50271657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278454-C-T

50271672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278416-T-A

50271674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278414-G-T

50271678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278410-T-C

http://identifiers.org/hco/19/GRCh38#50271683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44278405-C-A

http://identifiers.org/hco/19/GRCh38#50271684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44278404-C-A

50271702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278390-A-G

50271710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278382-G-A

50271710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278382-G-T

http://identifiers.org/hco/19/GRCh38#50271833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44278315-C-A

50271833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278315-C-T

50271930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44278229-A-G

50272491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278137-G-A

50272491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278137-G-C

50272491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278137-G-T

50272506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278115-G-A

50272506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278115-G-T

50272507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278114-G-A

50272507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278114-G-T

50272523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278097-T-A

50272523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44278097-T-C

http://identifiers.org/hco/19/GRCh38#50272553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44278068-C-A

50272583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44278038-G-A

50272583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44278038-G-T

50272602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44278019-A-G

50272602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44278019-A-T

50275533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44277215-C-T

50275609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44277134-T-C

50275638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44277091-G-A

50275722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44276966-A-T

50275743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44276929-T-C

50275836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44276814-A-T

50275855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44276793-T-C

50275897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44276750-T-A

50275897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44276750-T-C

http://identifiers.org/hco/19/GRCh38#50275914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44276729-A-C

50275914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44276729-A-G

50275914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44276729-A-T

50275950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44276694-G-A

50275950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44276694-G-T

http://identifiers.org/hco/19/GRCh38#50275982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44276657-C-A

50275982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44276657-C-T

50275988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44276651-C-T

50275998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44276639-G-T

50276130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, undefined
orthologous variants: 44276507-G-A

50276200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, undefined
orthologous variants: 44276437-T-C

50276208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44276429-G-T

50276687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44274999-C-G

50276687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44274999-C-T

50276690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44274996-G-A

50276690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44274996-G-T

http://identifiers.org/hco/19/GRCh38#50276697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44274989-C-A

50276697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44274989-C-T

50276715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44274972-C-G

50276715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44274972-C-T

50276875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44274812-G-T

50278131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44274546-T-A

50278143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44274534-G-A

50278194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44274483-C-G

50278194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44274483-C-T

http://identifiers.org/hco/19/GRCh38#50278209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44274468-C-A

50278209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: stop gained
orthologous variants: 44274468-C-T

http://identifiers.org/hco/19/GRCh38#50280130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44273753-C-A

50280372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44273511-G-A

50280372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44273511-G-T

http://identifiers.org/hco/19/GRCh38#50280448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44273486-C-A

50280448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44273486-C-T

50280508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44273458-T-C

http://identifiers.org/hco/19/GRCh38#50280527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44273437-A-C

50280527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44273437-A-G

http://identifiers.org/hco/19/GRCh38#50280823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44273258-C-A

50281225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44272983-T-C

50281360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44272851-A-G

50281423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44272794-G-A

50281452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44272774-T-C

50281452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44272774-T-G

http://identifiers.org/hco/19/GRCh38#50281453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44272773-C-A

http://identifiers.org/hco/19/GRCh38#50281491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44272738-C-A

50281492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44272737-T-C

50281495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44272734-A-G

50281519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44272712-A-G

50281522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron variant
orthologous variants: 44272709-G-T

50281627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44272613-G-T

http://identifiers.org/hco/19/GRCh38#50281744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44272496-C-A

50281744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44272496-C-T

50281780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44272460-G-A

50281780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense variant
orthologous variants: 44272460-G-T

http://identifiers.org/hco/19/GRCh38#50286387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44271465-C-A

50286387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44271465-C-G

50286388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44271464-T-A

http://identifiers.org/hco/19/GRCh38#50286391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44271461-C-A

50286391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44271461-C-T

50286426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44271421-G-T

50286436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44271410-T-C

50286506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44271348-G-A

50286506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44271348-G-T

50286608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44271246-G-A

50286692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 44271162-A-G

50286698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44271156-A-G

50286726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44271138-T-A

50286726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44271138-T-C

50286728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44271136-G-A

50286728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44271136-G-T

50286733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44271132-G-A

50286733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44271132-G-T

http://identifiers.org/hco/19/GRCh38#50286746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44271119-C-A

50286746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44271119-C-T

50289321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44265829-G-T

50289462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44265708-G-A

50289463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44265707-G-A

50289463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44265707-G-C

http://identifiers.org/hco/19/GRCh38#50290878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44264937-C-A

50290878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44264937-C-T

http://identifiers.org/hco/19/GRCh38#50290887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44264928-C-A

50290887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 44264928-C-T

50290908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44264907-C-T

50290945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44264870-C-G

50290945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44264870-C-T

http://identifiers.org/hco/19/GRCh38#50291125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44264639-C-A

50291143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44264622-T-C

50292115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263971-A-G

50292115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263971-A-T

50292157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263927-T-C

50292195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263910-G-A

50292195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263910-G-C

50292195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263910-G-T

50292206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263899-G-A

50292206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263899-G-C

50292206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263899-G-T

50292242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263858-C-G

50292403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263705-A-G

50292413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263695-C-T

50292426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263685-C-T

50292529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263611-G-A

http://identifiers.org/hco/19/GRCh38#50292704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44263497-A-C

http://identifiers.org/hco/19/GRCh38#50293257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44263128-C-A

50293257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44263128-C-T

50293387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44263052-G-T

50293693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44262851-C-T

50301554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44261244-G-T

50301564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44261234-A-G

50301590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44261208-G-T

http://identifiers.org/hco/19/GRCh38#50301624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44261192-C-A

50301640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44261176-T-C

50301688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44261126-G-A

50301722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44261092-G-A

50301790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44261024-C-G

50301790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44261024-C-T

50306899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44258084-G-C

50306899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44258084-G-T

http://identifiers.org/hco/19/GRCh38#50306974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44258024-C-A

50306974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44258024-C-T

50307797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44257640-G-A

50308101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44257345-G-A

50308193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44257250-G-C

50308236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44257207-T-A

50308272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44257176-A-G

50308544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256995-T-G

50308595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256946-G-A

50308595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256946-G-C

50308595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256946-G-T

50308663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256884-A-G

50308681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256859-T-A

50308681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256859-T-G

50308682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256858-G-A

50308682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256858-G-T

http://identifiers.org/hco/19/GRCh38#50308709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44256781-C-A

50308709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256781-C-G

50308709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256781-C-T

http://identifiers.org/hco/19/GRCh38#50308780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44256548-C-A

50308935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256286-G-A

50308935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256286-G-T

http://identifiers.org/hco/19/GRCh38#50308982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44256244-C-A

50308982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256244-C-G

50308982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256244-C-T

50308986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256240-T-C

50309213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256032-G-A

50309213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256032-G-C

http://identifiers.org/hco/19/GRCh38#50309250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44256006-C-A

50309250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44256006-C-T

50309276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44255983-A-G

50309402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44255890-G-A

50309402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44255890-G-T

50309465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44255854-T-A

50309523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44255817-T-C

http://identifiers.org/hco/19/GRCh38#50309577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44255803-C-A

50309577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44255803-C-G

50309577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44255803-C-T

50309663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44255762-C-G

50309733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44255689-G-T

http://identifiers.org/hco/19/GRCh38#50309758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44255664-C-A

http://identifiers.org/hco/19/GRCh38#50309798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44255625-C-A

50309798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44255625-C-T

50309855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44255589-G-A

50309855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44255589-G-T

http://identifiers.org/hco/19/GRCh38#50309857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44255587-C-A

50309857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44255587-C-T

http://identifiers.org/hco/19/GRCh38#50309930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#44255527-C-A

50309930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23212
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44255527-C-G